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OMEPRAZOLE EXTENDED-RE

Active
SPE2DP-26-T-4402Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

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Omeprazole extended-release capsules, 20 mg in 30-count units, are procured under solicitation SPE2DP-26-T-4402 for government use with a total requirement of 23,000 units across multiple contract line items. Each unit must be packaged in sealed containers that protect against damage and shipped in commercial exterior containers to ensure safe, low-cost delivery to designated government destinations. The product must be stored at controlled room temperature between 20 and 25 degrees Celsius and carries a non-extendable shelf life of 18 months. All packaging and labeling must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and conform to DLA packaging requirements including palletization and hazardous material handling per Fed-Std-313 and ASTM D3951 where applicable. The item is regulated by the FDA and requires supplier verification through EBS referral. Shipments must be sent by traceable means only, excluding parcel post, and deliveries are required FOB destination within five days of ship date. The original required delivery date for all orders is no later than August 4, 2026, with one contract line due by July 30, 2026. The contract includes multiple delivery addresses across Fort Lewis, Washington, and Watervliet Arsenal, New York, with strict adherence to unit of issue and quantity per unit pack specifications. The sole source manufacturers listed include Astra Pharmaceutical Products Inc, Sandoz Inc, Amerisource Health Services LLC, and Golden State Medical Supply Inc, with NDC numbers specified for each.

General Info

23,000 units of 20 mg omeprazole capsules to be delivered by August 2026 to specified military sites under strict packaging and FDA regulations.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSAView Agency

NAICS

325412 - Pharmaceutical Preparation ManufacturingView NAICS

Place of Performance

9141 SANSONE, FORT LEWIS, WA, 98433-9500, US

Set-Aside

NONE

Documents

(1)

SPE2DP-26-T-4402.pdf

PDF

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Timeline

PhaseSolicitation
Posted

Solicitation

Response Deadline

Submission deadline

Response Deadline

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
Contacts1 person available
OfficeUS
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
View Agency Profile
Office AddressUS
Contacts
MEGHAN SMINK
contact@example.gov
+1 (555) 000-0000

Full Description

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OMEPRAZOLE EXTENDED-RELEASE CAPSULES
OMEPRAZOLE EXTENDED-RELEASE CAPSULES, 20 MG,30'S
STORE AT USP CONTROLLED ROOM TEMPERATUR 20 DEGREES 25 DEGRESS CELCIUS
APPLICABLE TO ALL MEDICAL ACQUISITIONS:
PACKAGING AND PACKING SHALL BE COMMERCIAL AS
SPECIFIED IN THE PROCUREMENT DOCUMENT.
EACH COMPLETE UNIT SHALL BE PROPERLY PACKAGED
IN A SUITABLE SEALED UNIT CONTAINER CAPABLE
OF PROTECTING THE CONTENTS FROM DAMAGE AND/OR
BREAKAGE.
UNITS SHALL BE PACKED IN SUITABLE COMMERCIAL
EXTERIOR (SHIPPING) CONTAINERS (EXPORT WHEN
NECESSARY) WHICH SHALL INSURE ACCEPTANCE AND
SAFE DELIVERY BY COMMON OR OTHER CARRIER, AT
THE LOWEST RATE, TO POINT OF DELIVERY CALLED
FOR IN THE CONTRACT OR ORDER.
MATERIAL MUST BE MARKED IAW MEDICAL MARKING
STANDARD NO. 1. THIS SUPERCEDES ALL REFERENCES
TO MIL-STD-129.
COPIES OF MEDICAL MARKING STANDARD NO. 1
(MMS NO. 1) MAY BE OBTAINED BY CONTACTING DLA
TROOP SUPPORT VIA EMAIL TO fssb@dla.mil. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: https://www.dla.mil/Logistics-Operations/Packaging/
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
003 OBJECT TEXT ID ST
RA001: THIS DOCUMENT INCORPORATES TECHNICAL AND/OR QUALITY REQUIREMENTS
(IDENTIFIED BY AN 'R' OR AN 'I' NUMBER) SET FORTH IN FULL TEXT IN THE
DLA MASTER LIST OF TECHNICAL AND QUALITY REQUIREMENTS FOUND ON THE WEB
AT:
http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx
FOR SIMPLIFIED ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE SOLICITATION ISSUE DATE OR THE AWARD DATE CONTROLS. FOR LARGE ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE RFP ISSUE DATE APPLIES UNLESS A SOLICITATION AMENDMENT INCORPORATES A FOLLOW-ON REVISION, IN WHICH CASE THE AMENDMENT DATE CONTROLS.
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
This device or drug is regulated by the FDA. Note to Buyers: The contracting official shall send a referral in EBS to the product specialist for confirmation. Please include bidder name and bidder contact information, manufacturer name, manufacturer part number, and item description.
INCLUDE R2781 BT = 30 EA
SPE2DP-26-T-4402
SECTION B
0 OBJECT TEXT ID ST
RS013: Shelf-life requirement RS001 for a TYPE I (CODE K) item with a shelf life of 18 months (non-extendable) applies to this item.
SHALL BE MARKED IAW THE LATEST EDITION OF
THE MEDICAL MARKING STANDARD NO. 1.
MMS NO. 1 IS AVAILABLE ONLINE AT:
https://www.dla.mil/Logistics-Operations/Packaging/
ASTRA PHARMACEUTICAL PRODUCTS INC 1AK01 P/N NDC00186-0742-31 SANDOZ INC. 0THL4 P/N NDC00781-2868-31 AMERISOURCE HEALTH SERVICES, LLC 71M28 P/N NDC51407-0813-30 GOLDEN STATE MEDICAL SUPPLY, INC. 1HT23 P/N NDC60505-0065-00
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments% 2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0001 7017699745 0001 BT 4.000
NSN/MATERIAL:6505013142716
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
BULK BREAK POINT:
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
SPE2DP-26-T-4402
SECTION B
PR: 7017699745 PRLI: 0001 CONT’D
US
SHIP BY TRACEABLE MEANS. DO NOT USE PARCEL POST.
FREIGHT SHIPPING ADDRESS:
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
US
MARKFOR
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
US
M/F: (TCN) W91M1Z61800067
RDD: 193
PROJ: TP 3
SUPP ADD: W9046W SIG: C
FOR GOVERNMENT USE ONLY: (IPD) 12
DIC: A0A DIST: V ADV: 2A FC: Z9
Need Ship Date:00/00/0000 Original Required Delivery Date:08/04/2026
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments% 2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0002 7017701338 0001 BT 12.000
NSN/MATERIAL:6505013142716
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA-QUP:001
SPE2DP-26-T-4402
SECTION B
PR: 7017701338 PRLI: 0001 CONT’D
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313, PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025. IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
BULK BREAK POINT:
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
US
RDD 555 SHIPMENT. SHIP BY FASTEST TRACEABLE MEANS. DO NOT USE PARCEL POST.
FREIGHT SHIPPING ADDRESS:
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
US
MARKFOR
W91M1Z
0001 SF BN CO A GSB
AWCF SSF
9141 SANSONE
FORT LEWIS WA 98433-9500
US
M/F: (TCN) W91M1Z62110070
RDD: 555
PROJ: TP 1
SUPP ADD: W9046W SIG: C
SPE2DP-26-T-4402
SECTION B
PR: 7017701338 PRLI: 0001 CONT’D
FOR GOVERNMENT USE ONLY: (IPD) 02
DIC: A0A DIST: V ADV: 2A FC: Z9
Need Ship Date:00/00/0000 Original Required Delivery Date:08/04/2026
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments% 2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0003 7017693088 0001 BT 2.000
NSN/MATERIAL:6505013142716
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313, PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025. IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
SPE2DP-26-T-4402
SECTION B
PR: 7017693088 PRLI: 0001 CONT’D
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
BULK BREAK POINT:
W16DDS
W7NR USPFO ACTIVITY NY ARNG
1 BUFFINGTON ST B 145 AWCF SSF
WATERVLIET ARSENAL
WATERVLIET NY 12189-5000
US
SHIP BY TRACEABLE MEANS. DO NOT USE PARCEL POST.
FREIGHT SHIPPING ADDRESS:
W51JGX
0642 CS BN CO HQ & SPT CO
1 BUFFINGTON STREET BLDG 145
WATERVLIET NY 12189-0000
US
MARKFOR
W51JGX
0642 CS BN CO HQ & SPT CO
1 BUFFINGTON STREET BLDG 145
WATERVLIET NY 12189-0000
US
M/F: (TCN) W51JGX62100001
RDD:
PROJ: TP 3
SUPP ADD: W16DDS SIG: A
FOR GOVERNMENT USE ONLY: (IPD) 12
DIC: A0A DIST: ADV: 2A FC: 62
Need Ship Date:00/00/0000 Original Required Delivery Date:08/04/2026
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments%
SPE2DP-26-T-4402
SECTION B
PR: 7017655308 PRLI: 0001 CONT’D
2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0004 7017655308 0001 BT 5.000
NSN/MATERIAL:6505013142716
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313, PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025. IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313, PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025. IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT PKGING DATA-QUP:001
SPE2DP-26-T-4402
SECTION B
PR: 7017655308 PRLI: 0001 CONT’D
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
BULK BREAK POINT:
W16DDS
W7NR USPFO ACTIVITY NY ARNG
1 BUFFINGTON ST B 145 AWCF SSF
WATERVLIET ARSENAL
WATERVLIET NY 12189-5000
US
SHIP BY TRACEABLE MEANS. DO NOT USE PARCEL POST.
FREIGHT SHIPPING ADDRESS:
W16DDS
W7NR USPFO ACTIVITY NY ARNG
1 BUFFINGTON ST B 145 AWCF SSF
WATERVLIET ARSENAL
WATERVLIET NY 12189-5000
US
MARKFOR
W16DDS
W7NR USPFO ACTIVITY NY ARNG
1 BUFFINGTON ST B 145 AWCF SSF
WATERVLIET ARSENAL
WATERVLIET NY 12189-5000
US
M/F: (TCN) W16DDS62080022
RDD: 219
PROJ: TP 3
SUPP ADD: W9046W SIG: C
FOR GOVERNMENT USE ONLY: (IPD) 13
DIC: A0A DIST: V ADV: 2A FC: Z9
Need Ship Date:00/00/0000 Original Required Delivery Date:07/30/2026
DLA issues this document using the DoD authorized unit of issue, please refer to the following URL to determine the corresponding ANSI X12 unit of issue.
SPE2DP-26-T-4402
SECTION B
PR: 7017655309 PRLI: 0001 CONT’D
https://view.officeapps.live.com/op/view.aspx?src=https%3A%2F%2Fwww.dla.mil%2FPortals%2F104%2FDocuments% 2FDLMS%2FeApplications%2FLogDataAdmin%2FUnitofIssueandPurchaseUnit.xlsx&wdOrigin=BROWSELINK
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0005 7017655309 0001 BT 2.000
NSN/MATERIAL:6505013142716
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313, PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025. IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313, PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025. IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
SPE2DP-26-T-4402
SECTION B
PR: 7017655309 PRLI: 0001 CONT’D
PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313,
PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025.
IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH
FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE
WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT PKGING DATA-QUP:001
IF MATERIAL IS CONSIDERED HAZARDOUS IAW FED-STD-313, PACKAGE IN ACCORDANCE WITH TQ REQUIREMENT IP025. IF THE MATERIAL IS NOT CONSIDERED HAZARDOUS, IN ACCORDANCE WITH FED-STD-313, THE MATERIAL SHALL BE COMMERCIALLY PACKAGED IN ACCORDANCE WITH ASTM D3951.
All DLA Master List of Technical and Quality Requirements take precedence over ASTM D3951. Mark and label all packaging and packing in accordance with MIL-STD-129. The Unit of Issue (U/I) and Quantity per Unit Pack (QUP) will be as specified in the contract/purchase order. PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
BULK BREAK POINT:
W16DDS
W7NR USPFO ACTIVITY NY ARNG
1 BUFFINGTON ST B 145 AWCF SSF
WATERVLIET ARSENAL
WATERVLIET NY 12189-5000
US
SHIP BY TRACEABLE MEANS. DO NOT USE PARCEL POST.
FREIGHT SHIPPING ADDRESS:
W16DDS
W7NR USPFO ACTIVITY NY ARNG
1 BUFFINGTON ST B 145 AWCF SSF
WATERVLIET ARSENAL
WATERVLIET NY 12189-5000
US
MARKFOR
W16DDS
W7NR USPFO ACTIVITY NY ARNG
1 BUFFINGTON ST B 145 AWCF SSF
WATERVLIET ARSENAL
WATERVLIET NY 12189-5000
US
M/F: (TCN) W16DDS62080021
RDD: 219
PROJ: TP 3
SPE2DP-26-T-4402
SECTION B
PR: 7017655309 PRLI: 0001 CONT’D
SUPP ADD: W9046W SIG: C
FOR GOVERNMENT USE ONLY: (IPD) 13
DIC: A0A DIST: V ADV: 2A FC: Z9
Need Ship Date:00/00/0000 Original Required Delivery Date:07/30/2026
SPE2DP-26-T-4402 NSN/Part Number: 6505-01-314-2716 Quantity: 4 BT Purchase Request: 7017655308QTY: 5 Delivery: 5 days ADO

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ALUMINUM HYDROXIDE GEL
Solicitation # SPE2DP-26-T-4441
ALUMINUM HYDROXIDE GEL, USP, is procured under solicitation SPE2DP-26-T-4441 with a unit of issue as one bottle (1 BT or 16 OZ), requiring compliance with DLA’s Medical Marking Standard No. 1 and labeling per MMS No. 1A dated February 4, 2013, superseding MIL-STD-129. The product must have a mandatory 24-month shelf life, with no less than 21 months remaining from the date of manufacture to the date of government delivery. Packaging must meet commercial standards, ensuring each unit is sealed and protected against damage, and shipped in exterior containers suitable for safe transport via common carrier at the lowest cost to the destination specified in the contract. All items must be marked in accordance with DLA’s Medical Marking Standard, including NSN, manufacturer and CAGE code, date of manufacture, expiration date, contract number, and lot number. The item is regulated by the FDA, requiring referral via EBS to a product specialist before award, and must be accompanied by the manufacturer’s part number NDC00536-0091-85 from Watson Pharma Inc., with CAGE code 1DWF9. Delivery is FOB destination within 20 days, with zero variance in quantity and inspection and acceptance occurring at point of delivery. Packaging must conform to MIL-STD-2073-1E, and all technical and quality requirements are governed by the DLA Master List of Technical and Quality Requirements referenced in the document.
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HYDROGEN PEROXIDE TOPI
Solicitation # SPE2DP-26-T-4396
Hydrogen Peroxide Topical Solution, USP, is a 3% stabilized topical solution intended for external use only, with clear warnings against use in the eyes or over large body areas and a maximum usage duration of one week. Each unit is a 473-milliliter (16-fluid-ounce) bottle, requiring tight closure, storage at controlled room temperature, protection from freezing and excessive heat, and no shaking. Packaging and labeling must comply with Medical Marking Standard No. 1A dated February 4, 2013, superseding MIL-STD-129, and all units must be sealed in commercial containers suitable for transit and protected from damage. The product is regulated by the FDA and classified as a Type I (Code M) item with a non-extendable shelf life of 24 months. Suppliers must provide Safety Data Sheets (SDS) conforming to 29 C.F.R. 1910.1200 and Hazard Communication Standard (HCS) compliant labels as of June 1, 2015, and must train employees on these requirements. All packaging and shipping must meet commercial standards and ensure safe delivery at the lowest cost to the destination. The item is identified by NSN 6505-00-153-8480, with a purchase request number of 7017684184 and a quantity of 20 bottles. Delivery is FOB destination within 20 days, with zero variance allowed. Solicitation number SPE2DP-26-T-4396, posted August 2, 2026, requires response by August 10, 2026. Approved manufacturers include McKesson, Cardinal Health, and Medline Industries. The contract is administered by the Department of Defense’s Medical Supply Chain, with delivery to Pineville, LA, and point of contact Patrell Postell. All requisitions previously associated with DMLIIS Request ID 1721935 under ACC-L have been canceled without replacement, transitioning to ACCY.
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DIBUCAINE OINTMENT
Solicitation # SPE2DP-26-T-4418
Dibucaine Ointment USP is a topical pharmaceutical product containing 1 percent dibucaine as the active ingredient, formulated for rectal administration and external use only. It is supplied in a collapsible tube and includes a rectal applicator, with each unit of issue being a single package containing one ounce or 28 grams of ointment. The product must be stored at temperatures between 15 and 30 degrees Celsius (59 to 86 degrees Fahrenheit) and carries a non-extendable shelf life of 36 months, classified as a TYPE I (CODE Q) item. Packaging and marking must comply with the latest edition of the Medical Marking Standard No. 1 and MIL-STD-2073-1E, ensuring proper government logistics handling. The item is regulated by the FDA, and procurement requires a referral through EBS to verify compliance before award. This product is procured under solicitation SPE2DP-26-T-4418 with a required delivery within five days to Offutt AFB, zip 68113-1044, under FOB destination terms. Quantity is fixed at one package (PG) with zero variance allowed, and inspection and acceptance occur at the delivery point. The National Stock Number is 6505-00-299-9535, and the NDC code is 00536-1211-95. The supplier is The Harvard Drug Group, L.L.C., and the procurement is managed by the Department of Defense’s Medical Supply Chain Pharmacy FSA. Contract data specifies a response deadline of August 10, 2026, with technical and quality requirements governed by the DLA Master List of Technical and Quality Requirements. Covered Defense Information may apply under RD003, and removal of government identification from non-accepted supplies is required per RQ011.
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PETROLATUM, WHITE
Solicitation # SPE2DP-26-T-4447
The contract specifies the procurement of Petrolatum, White, USP, with a unit of issue of 1 TU equaling 28 mg, and a total quantity of 1 TU required. The item has a non-extendable shelf life of 36 months and must be packaged in accordance with the Medical Marking Standard No. 1, which supersedes MIL-STD-129, and all packaging must ensure protection against damage and compliance with commercial shipping standards for safe delivery to the destination. The material is not classified as hazardous under FED-STD-313 and must be commercially packaged per ASTM D3951, though any conflicting requirements from the DLA Master List of Technical and Quality Requirements take precedence. Labeling and marking of all containers must strictly follow the latest edition of Medical Marking Standard No. 1, and packaging must be palletized per RP001, using the designated unit pack configuration and ensuring the lowest freight cost to the specified delivery point. Delivery is required within five days of award, FOB destination, with zero variance allowed in quantity, and inspection and acceptance occur upon arrival. The item is to be shipped by the fastest traceable means, excluding parcel post, to the government address in Morrisville, NC, with explicit instructions to avoid using outdated or non-compliant marking systems. The solicitation is issued under contract SPE2DP-26-T-4447, with a required delivery date of August 4, 2026, and the item is identified by NSN 6505-00-254-5527 and NDC 53329-0068-01, supplied by Medline Industries, LP.
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ANESTHESIA SET, EPIDURA
Solicitation # SPE2DS-26-T-298A
The contract specifies the procurement of an epidural anesthesia set featuring a 20 gauge catheter and a 17 gauge Tuohy Schliff winged needle, with each package containing ten complete sets. The set comprises 29 components and must be delivered in its original packaging with a minimum shelf life of 12 months, ensuring no more than two months have elapsed between the date of manufacture and the date of delivery to the government. The item is identified by NSN 6515-01-323-6531 and is subject to stringent technical and quality requirements outlined in the DLA Master List of Technical and Quality Requirements, which governs compliance for both simplified and large acquisitions based on solicitation or award dates. Packaging must adhere to DLA standards, and non-accepted supplies must have all government identification removed prior to return. Bidders are required to clearly state the source and part number being supplied. The solicitation, issued under SPE2DS-26-T-298A, has a response deadline of August 10, 2026, with a required delivery within 20 days of award, and is managed by the Department of Defense’s Medical Supply Chain through the point of contact James Burke.
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PERMETHRIN CREAM RINSE
Solicitation # SPE2DP-26-T-4404
Permethrin Cream Rinse is a 1% w/v topical pharmaceutical product packaged in a 2 fluid ounce plastic squeeze bottle, each unit including a comb for application. The product has a 24-month shelf life, with a mandatory minimum of 21 months remaining at the time of receipt by the first government activity. It is regulated by the FDA and subject to strict medical acquisition standards, including commercial packaging requirements that ensure the unit is sealed and protected from damage, and shipments are placed in suitable exterior containers for safe transport at the lowest carrier rate. All items must be marked in compliance with Medical Marking Standard No. 1, replacing all references to MIL-STD-129. The product is hazardous and requires compliance with Federal Standard No. 313-E, mandating submission of current Safety Data Sheets (SDS) formatted per 29 C.F.R. 1910.1200 and appropriate Hazard Communication Standard labels prior to award. Each shipment must include a physical copy of the SDS, and suppliers must submit these documents to DLA.MSDS@DLA.MIL with a completed cover sheet. Packaging must meet 49 CFR and ICAO regulations for hazardous materials. Technical and quality requirements are governed by the DLA Master List, and the procurement is subject to Hazard Communication Standard updates. The NSN is 6505-01-256-4972, and the solicitation requires delivery of five units within five days of award, with the contract issued under SPE2DP-26-T-4404 by the Department of Defense, Medical Supply Chain Pharm FSA.
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ALBUTEROL SULFATE INHA
Solicitation # SPE2DP-26-T-4437
Albuterol Sulfate Inhalation Aerosol with HFA is a prescription-only medication for oral inhalation, with each actuation delivering 108 micrograms of albuterol sulfate equivalent to 90 micrograms of albuterol base, supplied in an 8.5-gram canister containing 200 metered doses. The product must be stored at room temperature between 59°F and 77°F, protected from extreme heat or cold, and must not be punctured, exposed to flames, or stored near heat sources, as temperatures above 120°F may cause the canister to burst. It is subject to a non-extendable 24-month shelf life and must be labeled with the National Stock Number, manufacturer name, date of manufacture, expiration date, contract number, and lot number. All packaging and marking must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and must be shipped in sealed commercial unit containers and approved shipping containers suitable for safe transport at the lowest rate to the delivery point specified. The product is regulated by the FDA and requires submission of Safety Data Sheets and Hazard Communication Standard-compliant labels as mandated by OSHA’s Globally Harmonized System, with supplier training on these requirements. Delivery is FOB destination within five days, with zero tolerance for quantity variance, and inspection and acceptance occur at the delivery point. The contract is issued under solicitation SPE2DP-26-T-4437 for a quantity of 12 units, with the National Stock Number 6505015436562, and references applicable DLA technical and quality requirements contained in the DLA Master List.
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CHLORINE TEST REAGE
Solicitation # SPE2DS-26-T-295L
The contract specifies the procurement of chlorine test reagent in powder pillow form, with each package containing 100 individual 10 mL samples, packaged as one unit of issue labeled PG. The product is designated by NSN 6550-01-460-7597 and is subject to strict technical and quality standards referenced in the DLA Master List of Technical and Quality Requirements, with compliance controlled by the revision in effect at the solicitation or award date. The item is classified as a TYPE I (CODE S) medical supply with a non-extendable shelf life of 60 months, and no more than eight months may have elapsed between the date of manufacture and delivery to the government. Packaging must meet commercial standards as outlined in Medical Marking Standard No. 1, which supersedes MIL-STD-129, and all labels must clearly display the date of manufacture, expiration or retest date, and the contract or lot number in accordance with MMS1C. The item must be securely packaged in sealed unit containers and shipped in commercial exterior containers suitable for safe transport via common carriers at the lowest possible rate to the designated delivery point. The procurement is issued under solicitation SPE2DS-26-T-295L, with a response deadline of August 10, 2026, and a delivery requirement within 20 days after award. The contracting activity is under the Department of Defense’s Medical Supply Chain, and all packaging, marking, and documentation must fully comply with the applicable DLA requirements for defense medical acquisitions.
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ZINC OXIDE OINTMENT
Solicitation # SPE2DP-26-T-4398
Zinc Oxide Ointment USP, 20% strength in 1-ounce collapsible tubes, is procured under contract SPE2DP-26-T-4398 with a total order of 100 tubes across nine line items, each designated by a unique CLIN and purchase request number. The product is classified as a topical skin protectant and must be stored at controlled room temperature not exceeding 30°C (86°F). Each tube contains 28.35 grams and is packaged as a single unit of issue (TU), with strict adherence to packaging standards including MIL-STD-129 and the Medical Marking Standard No. 1, which supersedes all other marking requirements. All packaging must comply with DLA’s Master List of Technical and Quality Requirements, with ASTM D3951 applying only if the material is non-hazardous per FED-STD-313; hazardous material must meet IP025 requirements. The item is regulated by the FDA, and bidders must be verified through an EBS referral. Shelf life is fixed at 36 months with no extension permitted, and the product must be marked with its NDC number (67777-0223-11) and manufacturer details (Dynarex Corp, P/N 1190). Delivery is FOB destination with zero variance allowance, inspection and acceptance occurring at the point of delivery. Shipments must use traceable freight methods only and avoid parcel post. Packaging must ensure protection from damage and conform to commercial standards, with palletization following RP001 guidelines. Eight delivery locations span military installations across North Carolina, Virginia, Louisiana, Massachusetts, and other states, with specified delivery dates ranging from July 15, 2026, to August 4, 2026. Unit price is fixed at $3.00 per tube across all line items, with total contract value reflecting aggregated quantities.
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MICONAZOLE NITRATE
Solicitation # SPE2DP-26-T-4428
Miconazole Nitrate Cream, USP 2% in a 1 oz tube is procured under solicitation SPE2DP-26-T-4428 with a unit of issue as a tube and a required shelf life of 36 months, of which no less than 31 months must remain from the date of manufacture to the date of delivery to the Government. The product must be manufactured by Taro Pharmaceuticals U.S.A., Inc. with NDC 51672-2001-02 and complies with all applicable FDA regulations. Packaging must adhere strictly to Commercial Packaging standards as specified in the DLA Master List of Technical and Quality Requirements, with each unit sealed in a protective container and shipped in commercial exterior containers suitable for safe transit at the lowest carrier rate. Marking must follow Medical Marking Standard No. 1A dated February 4, 2013, superseding MIL-STD-129, and all external labeling must conform to this standard. The item must be stored at controlled room temperature between 59°F and 86°F (15°C–30°C). Delivery is due within 20 days FOB destination, with no tolerance for quantity variance, and inspection and acceptance occur at the delivery point. The procurement is governed by DLA packaging and quality requirements, and all documentation, including packaging and labeling, must align with DLA’s Medical Marking Standard No. 1. The NSN is 6505010043508, and the purchase request number is 7017693914.
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SODIUM CHLORIDE INJECT
Solicitation # SPE2DP-26-T-4440
Sodium Chloride 0.9% Injection, USP, in 250 mL units, is procured under contract SPE2DP-26-T-4440 with a requirement for 4 packaging groups, each containing 24 bags, totaling 96 bags. The product must comply with all technical and quality specifications outlined in the DLA Master List of Technical and Quality Requirements, including packaging and marking standards per Medical Marking Standard No. 1, which supersedes MIL-STD-129. Each unit must be sealed in commercial-grade containers that protect against damage and breakage, and shipped in exterior containers suitable for safe delivery via common carrier at the lowest cost to the designated destination. The product is regulated by the FDA and must be marked with the NDC00264-7800-20 identifier or equivalent approved part numbers from approved manufacturers including B. Braun Medical Inc., Trillamed LLC, and Cardinal Health. The item has a non-extendable shelf life of 24 months and must be stored at room temperature (25°C), with limited tolerance for brief exposure up to 40°C; it must be protected from freezing and excessive heat. Delivery is required within five days FOB destination with zero variance tolerated, and inspection and acceptance occur upon delivery. All packaging and labeling must conform to MIL-STD-2073-1E, and the NSN is 6505-01-331-8945. The contracting official must submit a referral in EBS to confirm bidder and manufacturer details prior to award.
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NORETHINDRONE AND E
Solicitation # SPE2DP-26-T-4414
The contract specifies the procurement of Norethindrone and Ethinyl Estradiol Tablets USP, a hormonal contraceptive regulated by the FDA, in a standardized 28-tablet cycle format with three distinct active ingredient strengths: 7 tablets of 0.5 mg Norethindrone and 35 mcg Ethinyl Estradiol, 7 tablets of 0.75 mg and 35 mcg, and 7 tablets of 1 mg and 25 mcg, followed by 7 inert tablets per cycle. Each package unit consists of six 28-tablet cycles, totaling 168 tablets per package, with a required shelf life of 36 months from manufacture, ensuring no less than 31 months remain until delivery to the government. Packaging must comply strictly with Medical Marking Standard No. 1, superseding MIL-STD-129, and must be enclosed in sealed unit containers protected from damage, packed in commercial shipping containers suitable for safe transport at the lowest cost to the delivery point. The product is to be manufactured by TEVA PHARMACEUTICALS USA, INC., identified by NDC 00555-9012-58, and stored at 25°C (77°F) with allowable excursions between 15°C and 30°C. Delivery is required FOB destination within 20 days, with no tolerance for quantity variance. The contract, issued under solicitation SPE2DP-26-T-4414, references DLA’s Master List of Technical and Quality Requirements and mandates adherence to all applicable DLA packaging, marking, and logistics standards including MIL-STD-2073-1E for preparation. The contracting officer must confirm bidder and manufacturer details via EBS referral prior to award.
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SODIUM CHLORIDE INJECT
Solicitation # SPE2DP-26-T-4397
Sodium Chloride Injection USP 0.9% in 1000ml plastic bags, latex free, is being procured under solicitation SPE2DP-26-T-4397 with a unit of issue defined as one package of twelve units. The product must comply with strict technical and quality requirements as defined in the DLA Master List of Technical and Quality Requirements and must adhere to Medical Marking Standard No. 1, superseding all references to MIL-STD-129. Packaging must be commercial-grade, sealed, and designed to protect against damage and breakage, with exterior shipping containers ensuring safe and cost-effective delivery to the destination point. The item is regulated by the FDA and has a non-extendable shelf life of 30 months, with storage required at controlled room temperature between 20°C and 25°C, protection from excessive heat and freezing, and segregation from incompatible materials. The sole approved manufacturer is B. Braun Medical Inc with part number NDC00264-5802-00, though other vendors may submit bids under their respective part numbers. The contract specifies a firm quantity of twelve units per package, with zero variance permitted, and requires delivery within five days FOB destination to Carville, LA 70721. Inspection and acceptance occur at the delivery point. All markings, documentation, and compliance must align with current DLA standards, and buyers must refer specific bidder and manufacturer details to the DLA product specialist via EBS for confirmation prior to award.
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PSYLLIUM HYDROPHILIC M
Solicitation # SPE2DP-26-T-4405
The contract is for the procurement of Psyllium Hydrophilic Mucilloid in 12-gram packets, each containing 25 mg of potassium and 5 mg of sodium, packaged in units of 30 packets per case. This product is regulated by the FDA and must be supplied with its manufacturer’s part number NDC37000-0740-87, sourced from Procter & Gamble Distributing LLC. The item has a non-extendable shelf life of 24 months and must comply with DLA’s technical and quality requirements as defined in the DLA Master List, with packaging and marking strictly governed by Medical Marking Standard No. 1, which supersedes all references to MIL-STD-129. Packaging must meet MIL-STD-2073-1E and DLA-specific packaging requirements, ensuring secure, commercial-grade containment capable of protecting contents during transit. Delivery is FOB destination with no tolerance for quantity variance, and items must be shipped within five days of contract award using the fastest traceable means—parcel post is prohibited. The delivery address is a Navy vessel in FPO AP 96675, with specific shipping and marking instructions governed by DLA’s logistics protocols. The NSN is 6505-01-719-3181, and the contract number is SPE2DP-26-T-4405, with an original required delivery date of August 4, 2026. All bids must include the supplier and manufacturer details for FDA referral through EBS prior to award.
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LUBRICANT, SURGICAL
Solicitation # SPE2DP-26-T-4417
The contract is for surgical lubricant, a sterile, latex-free, water-soluble jelly containing parabens, with each foil packet containing 2.7 grams and packaged in boxes of 144 packets as the unit of issue. The product must comply with strict technical and quality requirements outlined in the DLA Master List, and all packaging and marking must adhere to the Medical Marking Standard No. 1, which supersedes MIL-STD-129. The item has a non-extendable shelf life of 36 months and must be stored at 20°C to 25°C (68°F to 77°F). It is regulated by the FDA and classified as a TYPE I (CODE Q) item with specific shelf-life controls. The supplier, MEDLINE INDUSTRIES, LP, must provide the item under part number MDS032273H, and the NSN is 6505-01-626-5774. The contract requires delivery of one box within 20 days to a designated military destination, with FOB destination terms and zero variance permitted on quantity. All packaging must be commercial-grade, sealed, and designed for safe transit with minimal cost to ensure unharmed delivery. The item must be marked according to MMS No. 1, and transportation details are governed by DLAD procedural notes. The contract is issued under solicitation SPE2DP-26-T-4417 with a required delivery date of August 4, 2026, and the point of contact is Nicholas Quigley of the Department of Defense’s Medical Supply Chain.
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OMEPRAZOLE EXTENDED-RE
Solicitation # SPE2DP-26-T-4416
The contract specifies the procurement of 20 mg extended-release omeprazole capsules in 90-count bottles, identified by NSN 6505016247068 and manufacturer part number NDC00781-2868-92 from Sandoz Inc. Each unit must be packaged in commercial-grade sealed containers that protect against damage, with outer shipping containers ensuring safe, low-cost delivery to listed government destinations under FOB destination terms. A minimum of 21 months of shelf life must remain at delivery, with a total shelf life of 24 months that is non-extendable. All packaging, labeling, and marking must comply with Medical Marking Standard No. 1, which supersedes MIL-STD-129, and palletization must adhere to DLA Packaging Requirements for Procurement. The product is regulated by the FDA and requires pre-award referral for confirmation. Shipments must use traceable transportation methods and explicitly prohibit parcel post. Deliveries are scheduled across multiple CLINs totaling 57 units, with a mandatory delivery window of five days and no variance allowed in quantity. All items must be labeled and stored at controlled room temperature, with packaging materials and methods governed by DLA’s Master List of Technical and Quality Requirements, which take precedence over ASTM D3951. Shipping addresses include military facilities at Fort Bragg, North Carolina, and APO AP, with required point-of-contact and program tracking information provided for government use.
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SUMATRIPTAN SUCCINATE
Solicitation # SPE2DP-26-T-4415
Sumatriptan Succinate Tablets, 100 mg, are supplied in a bottle of nine tablets and are indicated for the acute treatment of migraine with or without aura in adults. The product must be stored at controlled room temperature between 20 to 25°C (68 to 77°F) and protected from light, in compliance with USP standards. The item is regulated by the FDA and subject to strict shelf-life requirements: it has a non-extendable shelf life of 24 months as a Type I CODE M item, and must be marked according to the latest edition of Medical Marking Standard No. 1 and MIL-STD-129 for packaging and labeling. Packaging and palletization must adhere to DLA’s Packaging Requirements for Procurement and MIL-STD-2073-1E, with no tolerance for quantity variance. The contract specifies delivery FOB destination within 20 days, with inspection and acceptance occurring at the destination. The supplier is identified as MYLAN PHARMACEUTICALS INC with NDC 00378-5632-59, and the item is procured under NSN 6505-01-727-8704. Delivery is to a U.S. military address in APO AE 09094-3219, with freight originating from Ramstein, Germany. The solicitation number is SPE2DP-26-T-4415, with a required delivery date of August 4, 2026, and bid responses due by August 10, 2026. Technical and quality requirements are governed by the DLA Master List, and the contracting official must submit a referral through EBS for FDA product validation prior to award.
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SODIUM CHLORIDE INJ
Solicitation # SPE2DP-26-T-4446
Sodium Chloride Injection in 10 mL disposable syringes, preservative-free and latex-free, is being procured under contract SPE2DP-26-T-4446 with a total quantity of 2 packing groups, each containing 30 syringes for a total of 60 units. The product is regulated by the FDA and must comply with all applicable DLA Master List of Technical and Quality Requirements, including medical packaging and marking standards as defined in Medical Marking Standard No. 1, which supersedes MIL-STD-129. Packaging must be commercial grade, sealed to prevent damage or breakage, and placed in exterior shipping containers suitable for safe transport at the lowest carrier rate to the designated delivery point. The item has a non-extendable shelf life of 24 months and must be labeled accordingly. Delivery is FOB destination within 20 days of award, with no tolerance for quantity variance. Freight must be shipped by traceable means, excluding parcel post, to the specified delivery location at Watervliet Arsenal, New York. The supplier, AmerisourceBergen Drug Corp with part number 106346, must adhere to all applicable hazardous material guidelines under Fed-Std-313 and ASTM D3951 where relevant, though DLA requirements override any conflicting standards. All packaging, labeling, and palletization must conform to RP001 and the latest DLA packaging directives.
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