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SUMATRIPTAN SUCCINATE

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SPE2DP-26-T-4339Federal

Contract Overview

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

AI Contract Overview

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Sumatriptan Succinate Tablets, 100 mg in bottles of nine tablets, are procured under contract SPE2DP-26-T-4339 for acute treatment of migraines with or without aura in adults. The product must be stored at 20 to 25°C (68 to 77°F), protected from light, and carries a non-extendable 24-month shelf life as a Type I (Code M) item. Packaging and labeling must comply with MIL-STD-2073-1E, MIL-STD-129, and the latest Medical Marking Standard No. 1, with palletization following DLA Packaging Requirements. The item is regulated by the FDA and requires confirmation via EBS referral before award. Delivery is FOB destination within five days, with zero quantity variance allowed, and inspection and acceptance occur at the delivery point. Three separate CLINs specify delivery to APO AE 09094-3219 and JBER AK 99506, with total quantities of one bottle each for two entries and five bottles for the third, all under the same NSN 6505017278704. The contract references DLA technical and quality requirements, including RD003 for covered defense information, and mandates adherence to specified marking and shipping protocols. The solicitation was posted on July 28, 2026, with a response deadline of August 3, 2026, and required delivery dates range from July 29 to July 30, 2026.

General Info

100 mg sumatriptan succinate tablets, 7 bottles total, FOB destination, FDA-regulated, strict storage and labeling requirements.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSAView Agency

NAICS

325411 - Medicinal and Botanical ManufacturingView NAICS

Place of Performance

UNIT 2497 CP 011 496 371 46 2418, APO, AE, 09094-3219, US

Set-Aside

NONE

Documents

(1)

SPE2DP-26-T-4339.pdf

PDF

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Timeline

PhaseSolicitation
Posted

Solicitation

Response Deadline

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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
Vanesa M Carbo Acevedo
contact@example.gov
+1 (555) 000-0000

Full Description

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SUMATRIPTAN SUCCINATE TABLETS
SUMATRIPTAN SUCCINA
SUMATRIPTAN SUCCINATE TABLETS, 100MG BOTTLE OF 9 TABLETS. STORE AT 20
TO 25 C (68 TO 77 F). [SEE USP CONTROLLED ROOM TEMPERATURE.]PROTECT
FROM LIGHT. INDICATED FOR THE ACUTE TREATMENT OF MIGRAINE WITH OR
WITHOUT AURA IN ADULTS.
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.
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
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.
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
Shall be marked IAW the latest edition of Medical Marking Standard No. 1 https://www.dla.mil/Logistics-Operations/Packaging/
GOLDEN STATE MEDICAL SUPPLY, INC. 1HT23 P/N NDC51407-0013-09 MYLAN PHARMACEUTICALS INC 3KJG9 P/N NDC00378-5632-59
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
SPE2DP-26-T-4339
SECTION B
PR: 7017649215 PRLI: 0001 CONT’D
CLIN PR PRLI UI QUANTITY UNIT PRICE TOTAL PRICE.
0001 7017649215 0001 BT 1.000
NSN/MATERIAL:6505017278704
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA MIL-STD-2073-1E
QUP:001 PRES MTHD:ZZ CLNG/DRY:Z PRESV MAT:ZZ
WRAP MAT:ZZ CUSH/DUNN MAT:ZZ CUSH/DUNN THKNESS:Z
UNIT CONT:ZZ OPI:M
INTRMDTE CONT:ZZ INTRMDTE CONT QTY:ZZZ
PACK CODE:Z PACKING LEVEL: B
MARKING SHALL BE IN ACCORDANCE WITH MIL-STD-129.
SPECIAL MARKING CODE:ZZ -ZZ Special Requirements
PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
Shall be marked IAW the latest edition of Medical Marking Standard No. 1 https://www.dla.mil/Logistics-Operations/Packaging/
PARCEL POST ADDRESS:
FM5612
FM5612 86 MDSS SGSM
UNIT 2497 CP 011 496 371 46 2418
APO AE 09094-3219
US
FOR TRANSPORTATION SEE DLAD DLAD PROC NOTE C19. FOR FIRST DESTINATION TRANSPORTATION SEE DLAD PROC NOTE
C20 AND CONTRACT
FREIGHT SHIPPING ADDRESS:
FM5612
FM5612 86 MDSS SGSM
UNIT 3219BLDG 2497 CP 0110114963714
LINCOLN BLVD RAMSTEIN FLUGPLATZ
RAMSTEIN 66877
DE
M/F: (TCN) FM561262080414
RDD:
PROJ: TP 3
SUPP ADD: SIG: A
FOR GOVERNMENT USE ONLY: (IPD) 13
SPE2DP-26-T-4339
SECTION B
PR: 7017649215 PRLI: 0001 CONT’D
DIC: A01 DIST: ADV: 2A FC: 6B
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.
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 7017631641 0001 BT 1.000
NSN/MATERIAL:6505017278704
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA MIL-STD-2073-1E
QUP:001 PRES MTHD:ZZ CLNG/DRY:Z PRESV MAT:ZZ
WRAP MAT:ZZ CUSH/DUNN MAT:ZZ CUSH/DUNN THKNESS:Z
UNIT CONT:ZZ OPI:M
INTRMDTE CONT:ZZ INTRMDTE CONT QTY:ZZZ
PACK CODE:Z PACKING LEVEL: B
MARKING SHALL BE IN ACCORDANCE WITH MIL-STD-129.
SPECIAL MARKING CODE:ZZ -ZZ Special Requirements
PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
Shall be marked IAW the latest edition of Medical Marking Standard No. 1 https://www.dla.mil/Logistics-Operations/Packaging/
PKGING DATA MIL-STD-2073-1E QUP:001 PRES MTHD:ZZ CLNG/DRY:Z PRESV MAT:ZZ WRAP MAT:ZZ CUSH/DUNN MAT:ZZ CUSH/DUNN THKNESS:Z UNIT CONT:ZZ OPI:M INTRMDTE CONT:ZZ INTRMDTE CONT QTY:ZZZ PACK CODE:Z PACKING LEVEL: B MARKING SHALL BE IN ACCORDANCE WITH MIL-STD-129. SPECIAL MARKING CODE:ZZ -ZZ Special Requirements
PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a
SPE2DP-26-T-4339
SECTION B
PR: 7017631641 PRLI: 0001 CONT’D
shelf life of 24 months (non-extendable) applies to this item.
Shall be marked IAW the latest edition of Medical Marking Standard No. 1 https://www.dla.mil/Logistics-Operations/Packaging/
PARCEL POST ADDRESS:
FM5000
FM5000 673 MDSS SGSM
5250 GIBSON AVE BLDG 5250
JBER AK 99506-4400
US
FOR TRANSPORTATION SEE DLAD DLAD PROC NOTE C19. FOR FIRST DESTINATION TRANSPORTATION SEE DLAD PROC NOTE
C20 AND CONTRACT
FREIGHT SHIPPING ADDRESS:
FM5000
FM5000 673 MDSS SGSM
CP 907 552 8846
5250 GIBSON AVE BLDG 5250
JBER AK 99506
US
M/F: (TCN) FM500062050059
RDD:
PROJ: TP 1
SUPP ADD: SIG: A
FOR GOVERNMENT USE ONLY: (IPD) 03
DIC: A01 DIST: ADV: 2A FC: 6B
Need Ship Date:00/00/0000 Original Required Delivery Date:07/29/2026
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 7017651738 0001 BT 5.000
NSN/MATERIAL:6505017278704
DELIVERY (IN DAYS):0005
DELIVER FOB: DESTINATION
QTY VARIANCE: PLUS 0% MINUS 0%
INSPECTION POINT: DESTINATION
SPE2DP-26-T-4339
SECTION B
PR: 7017651738 PRLI: 0001 CONT’D
ACCEPTANCE POINT: DESTINATION
PREP FOR DELIVERY:
PKGING DATA MIL-STD-2073-1E
QUP:001 PRES MTHD:ZZ CLNG/DRY:Z PRESV MAT:ZZ
WRAP MAT:ZZ CUSH/DUNN MAT:ZZ CUSH/DUNN THKNESS:Z
UNIT CONT:ZZ OPI:M
INTRMDTE CONT:ZZ INTRMDTE CONT QTY:ZZZ
PACK CODE:Z PACKING LEVEL: B
MARKING SHALL BE IN ACCORDANCE WITH MIL-STD-129.
SPECIAL MARKING CODE:ZZ -ZZ Special Requirements
PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
Shall be marked IAW the latest edition of Medical Marking Standard No. 1 https://www.dla.mil/Logistics-Operations/Packaging/
PKGING DATA MIL-STD-2073-1E QUP:001 PRES MTHD:ZZ CLNG/DRY:Z PRESV MAT:ZZ WRAP MAT:ZZ CUSH/DUNN MAT:ZZ CUSH/DUNN THKNESS:Z UNIT CONT:ZZ OPI:M INTRMDTE CONT:ZZ INTRMDTE CONT QTY:ZZZ PACK CODE:Z PACKING LEVEL: B MARKING SHALL BE IN ACCORDANCE WITH MIL-STD-129. SPECIAL MARKING CODE:ZZ -ZZ Special Requirements
PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
Shall be marked IAW the latest edition of Medical Marking Standard No. 1 https://www.dla.mil/Logistics-Operations/Packaging/
PKGING DATA MIL-STD-2073-1E QUP:001 PRES MTHD:ZZ CLNG/DRY:Z PRESV MAT:ZZ WRAP MAT:ZZ CUSH/DUNN MAT:ZZ CUSH/DUNN THKNESS:Z UNIT CONT:ZZ OPI:M INTRMDTE CONT:ZZ INTRMDTE CONT QTY:ZZZ PACK CODE:Z PACKING LEVEL: B MARKING SHALL BE IN ACCORDANCE WITH MIL-STD-129. SPECIAL MARKING CODE:ZZ -ZZ Special Requirements
PALLETIZATION SHALL BE IN ACCORDANCE WITH RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
Shall be marked IAW the latest edition of Medical Marking Standard No. 1 https://www.dla.mil/Logistics-Operations/Packaging/
PARCEL POST ADDRESS:
FM5612
SPE2DP-26-T-4339
SECTION B
PR: 7017651738 PRLI: 0001 CONT’D
FM5612 86 MDSS SGSM
UNIT 2497 CP 011 496 371 46 2418
APO AE 09094-3219
US
FOR TRANSPORTATION SEE DLAD DLAD PROC NOTE C19. FOR FIRST DESTINATION TRANSPORTATION SEE DLAD PROC NOTE
C20 AND CONTRACT
FREIGHT SHIPPING ADDRESS:
FM5612
FM5612 86 MDSS SGSM
UNIT 3219BLDG 2497 CP 0110114963714
LINCOLN BLVD RAMSTEIN FLUGPLATZ
RAMSTEIN 66877
DE
M/F: (TCN) FM561262080792
RDD:
PROJ: TP 3
SUPP ADD: SIG: A
FOR GOVERNMENT USE ONLY: (IPD) 13
DIC: A01 DIST: ADV: 2A FC: 6B
Need Ship Date:00/00/0000 Original Required Delivery Date:07/30/2026
SPE2DP-26-T-4339 NSN/Part Number: 6505-01-727-8704 Quantity: 1 BT Purchase Request: 7017631641QTY: 1 Delivery: 5 days ADO

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SUMATRIPTAN SUCCINATESumatriptan Succinate Tablets, 100mg in bottles of nine tablets, are being procured under solicitation SPE2DP-26-T-4284 by the Department of Defense’s Medical Supply Chain Pharmaceutical FSA for delivery to Joint Base Elmendorf-Richardson in Alaska. The item is regulated by the FDA and must be stored at 20 to 25°C (68 to 77°F), protected from light, with a non-extendable shelf life of 24 months as a Type I (Code M) item. The contract specifies delivery within five days of order, FOB destination, with inspection and acceptance occurring at the delivery point. Packaging must adhere to MIL-STD-2073-1E and be palletized per DLA’s RP001 requirements, with labeling and marking fully compliant with MIL-STD-129 and the latest Medical Marking Standard No. 1, including mandatory 2D Data Matrix barcodes. The unit of issue is a bottle, and the sole line item quantity is one bottle, with an estimated value of $18.77 based on prior procurement history. The NSN is 6505-01-727-8704, and the manufacturers listed are Mylan Pharmaceuticals Inc. and Golden State Medical Supply, Inc., with respective NDC codes. All supplies must be free of government identification upon rejection and comply with covered defense information requirements under RD003 and safeguards for cyber incident reporting under 252.204-7012. Invoicing must be submitted through Wide Area WorkFlow, and contractors must adhere to all applicable FAR clauses including 52.213-4 for simplified acquisitions, 52.216-1 with Alternate I for contract type, and provisions on hazardous materials, trafficking in persons, employment eligibility, and sustainable products. Offerors must complete required representations in Section K regarding small business status, UEI and CAGE codes, and compliance with prohibitions on covered telecommunications equipment, though no completed responses are provided in the solicitation. Proposals must be submitted electronically via DIBBS by August 3, 2026, using SF-18, with no page limits specified. The contract includes no option quantities, and the place of performance is fixed at the specified JBER address.
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NAICS: 325411
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KETOROLAC TROMETHAMINEKETOROLAC TROMETHAMINE INJECTION, USP 15 MG PER ML in prefilled syringes, packaged 24 per unit, is being procured under solicitation SPE2DP-26-T-4270 with a required delivery of five days to Fort Bragg, North Carolina. The product must comply with DLA’s Master List of Technical and Quality Requirements including shelf-life standards of 24 months, non-extendable, and packaging guidelines as per Medical Marking Standard No. 1, which supersedes MIL-STD-129. All packaging must protect against damage, be commercially sealed, and meet export shipping requirements where applicable. The item is labeled with NDC 76045-0107-10 and is manufactured by FRESENIUS KABI, LLC. The supply must adhere to federal hazardous material handling regulations under OSHA’s revised Hazard Communication Standard effective June 1, 2015, requiring submission of Safety Data Sheets and compliant labeling in accordance with 29 C.F.R. 1910.1200 prior to award. Employee training on these new safety standards is mandatory. Shipments must be sent via the fastest traceable means, excluding parcel post, and palletization must follow DLA’s RP001 packaging requirements. The contract specifies a zero percent quantity variance, acceptance at destination, and delivery to a secure government facility at Fort Bragg with strict marking and documentation protocols. The required delivery date is July 27, 2026, and all packaging and labeling must reflect current DLA and federal compliance standards without exception.
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NAICS: 325411
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MORPHINE SULFATE INMorphine Sulfate Injection 10 mg/mL in a 1x10 NEXJECT configuration, designated as a DEA Schedule II controlled substance, is being procured under solicitation SPE2DP-26-T-4277 with a total quantity of 3 packages, each containing 10 units. The item has a non-extendable shelf life of 18 months and must be stored at controlled room temperature. Packaging and labeling must comply with Medical Marking Standard No. 1, which supersedes MIL-STD-129, and all packaging must meet DLA’s procurement requirements and be commercial in nature, ensuring protection against damage during transport. The product is regulated by the FDA and requires confirmation through EBS referral by the contracting official prior to award. The manufacturer is Pfizer Inc., with NDC 00409-1893-23, and delivery is required FOB destination within five days of award to the specified address at Joint Base Elmendorf-Richardson, Alaska. The unit of issue is a package of 10, and no quantity variance is permitted. Transportation logistics are governed by DLA procedural notes C19 and C20, and the item must be marked and palletized according to DLA standards. All technical and quality requirements referenced by R or I numbers are incorporated from the DLA Master List, with the applicable revision controlled by the solicitation issue date.
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NAICS: 325411
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Chemical Detection Chip ManufacturingThe contract mandates the manufacture of chemical detection chips designed to detect ammonia concentrations within a precise range of 2.0 to 50.0 parts per million, with each unit incorporating ten reagent-filled capillaries calibrated during production to ensure accuracy and consistency. The chips must be engineered to maintain performance integrity over a two-year shelf life under standard storage conditions, requiring strict quality control throughout the fabrication process to guarantee reliability and longevity. Production must adhere to industry standards for analytical sensor fabrication, with calibration protocols documented and verified to meet the specified detection thresholds. The solicitation, issued under NAICS code 325411 for chemical and chemical products manufacturing, is structured as a subcontract within the Department of Defense’s Medical Supply Chain FSH framework. Performance is required at the APO location with ZIP code 09094-3219, indicating deployment to military or overseas operational sites where rapid, portable ammonia detection is critical for safety and environmental monitoring. The response deadline is set for July 30, 2026, with the solicitation posted on July 23, 2026, allowing a seven-day window for submissions through the DIBBS platform. All deliverables must be fully compliant with defense procurement technical and logistical requirements.
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NAICS: 424210
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SUNSCREEN PREPARATIONThe contract is for a topical sunscreen preparation containing 4.5% titanium dioxide and 4% zinc oxide with an SPF of 50, designed for outdoor use and labeled as sweat and water-resistant for 80 minutes, hypoallergenic, oil-free, PABA-free, and biodegradable. Each unit of issue is a package containing 24 tubes of 3 ounces, with a total shelf life of 24 months and a minimum of 21 months remaining at time of delivery to the first government activity. Storage must be maintained between 15°C and 30°C (59°F and 86°F) in a cool, dry environment. The product is regulated by the FDA and must comply with all DLA Master List of Technical and Quality Requirements, which take precedence over commercial standards like ASTM D3951. Packaging must adhere to Medical Marking Standard No. 1, superseding MIL-STD-129, and all units must be sealed and shipped in commercially appropriate containers that ensure safe delivery via common carrier at the lowest cost to the specified delivery points. Palletization must follow DLA packaging requirements, and shipment must occur by the fastest traceable means, excluding parcel post. The material is not classified as hazardous under FED-STD-313, so commercial packaging per ASTM D3951 applies unless overridden by stricter DLA requirements. Three separate delivery line items exist, totaling four pallets, with delivery addresses at military installations in Massachusetts, North Carolina, and aboard the USS Gridley via FPO. All deliveries are FOB destination with zero quantity variance, inspected and accepted at the delivery point, with required delivery dates ranging from July 29 to July 30, 2026. The solicitation number is SPE2DP-26-T-4340, with a response deadline of August 3, 2026.
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NAICS: 325412
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ZINC OXIDE OINTMENTZINC OXIDE OINTMENT USP, containing 20% zinc oxide in a 1-ounce collapsible tube weighing 28.35 grams, is procured as a topical skin protectant under contract SPE2DP-26-T-4335. The item is regulated by the FDA and must comply with all applicable DLA Master List of Technical and Quality Requirements, including packaging standards per MIL-STD-129 and DLA Packaging Requirements for Procurement RP001. The product requires storage at controlled room temperature not exceeding 30°C (86°F) and has a non-extendable shelf life of 36 months as a TYPE I (CODE Q) item. All packaging must be marked in accordance with the latest Medical Marking Standard No. 1 and labeled with the NDC number 67777-0223-11. The unit of issue is the tube (TU), and no variance in quantity is permitted. The contract includes two line items totaling 14 tubes: 10 tubes delivered to a location in Richmond, Virginia, and 4 tubes delivered to Melrose, Massachusetts. Both deliveries are FOB destination with a five-day delivery window and must be shipped via traceable means—parcel post is prohibited. Packaging must adhere to ASTM D3951 if not classified as hazardous under FED-STD-313, but DLA requirements override any conflicting standards. Palletization follows RP001 guidelines, and all shipments must include proper government identification markings. The original required delivery dates are July 29, 2026, and July 30, 2026, respectively. The contract specifies a unit price of $1.00 per tube with no total price variation, and it is managed by the Department of Defense’s Medical Supply Chain Pharm FSA, with James McCullough as the primary point of contact.
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NAICS: 325412
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ZOLMITRIPTAN TABLETZolmitriptan tablets, 2.5 mg film-coated, are supplied in blister packs containing six tablets per package, with the unit of issue defined as a package of six units. The product must be stored at controlled room temperature and marked in accordance with the latest edition of the Medical Marking Standard No. 1, adhering to DLA packaging requirements and technical quality standards as outlined in the DLA Master List of Technical and Quality Requirements. The item is classified as a Type I (Code Q) drug with a non-extendable shelf life of 36 months, and all supplies must comply with removal of government identification if not accepted, with potential application of Covered Defense Information protocols. The contract specifies two manufacturer part numbers—NDC71626-0101-06 from Medstone Pharma LLC and NDC60846-0130-30 from Amneal Pharmaceuticals of New York, LLC—both subject to FDA regulation and requiring prior confirmation via EBS referral by the contracting official. The delivery instruction requires FOB destination within 20 days, with no variance allowed in quantity, inspection and acceptance occurring at the delivery point, and packaging must meet MIL-STD-2073-1E standards. The contract, issued under solicitation SPE2DP-26-T-4332, has a posted date of July 28, 2026, and a response deadline of August 3, 2026, with three packages totaling 18 tablets ordered at $3.00 per package. The item is linked to NSN 6505015232352 and classified under NAICS code 325412 for pharmaceutical manufacturing.
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NAICS: 423450
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ATROPINE SULFATE INAtropine Sulfate Injection, USP, is a sterile, nonpyrogenic, preservative-free, and non-DEHP product supplied in a 5 mL single-dose syringe with a 20-gauge by 1.5-inch protected needle featuring a male Luer lock adapter. Each milliliter contains 0.1 mg of atropine sulfate monohydrate and 9 mg of sodium chloride, resulting in a total of 0.5 mg of atropine per syringe. The medication is indicated for subcutaneous, intramuscular, or intravenous administration and is labeled RX only. The product must be stored at controlled room temperature between 20°C and 25°C (68°F to 77°F) and has a non-extendable shelf life of 24 months. Packaging and labeling must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and all DLA Master List of Technical and Quality Requirements take precedence over commercial packaging standards. The product is regulated by the FDA and is supplied by Pfizer Inc with NDC code 00409-4910-34. The contract, issued under solicitation number SPE2DP-26-T-4325, requires delivery of one pallet (PG) containing ten units to Fort Bragg, North Carolina, within 20 days of order placement, FOB destination. No quantity variance is permitted, and inspection and acceptance occur at the delivery point. The material is not classified as hazardous under FED-STD-313 and must be commercially packaged in accordance with ASTM D3951, unless overridden by DLA requirements. All packaging must be marked and labeled per DLA specifications, palletized as per RP001, and shipped via traceable means, excluding parcel post. The delivery is mandated for July 29, 2026, with the contract awarded to the Department of Defense, Medical Supply Chain Pharm FSA, and all technical, quality, and packaging specifications are governed by the DLA Master List in effect on the solicitation issue date. A referral must be sent via EBS to confirm bidder and manufacturer details prior to award.
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LIDOCAINE HYDROCHLOLidocaine Hydrochloride and Epinephrine, USP, is a parenteral injectable pharmaceutical product containing a 2 percent concentration of lidocaine hydrochloride and a 1:50,000 dilution of epinephrine bitartrate, supplied in 1.7 mL single-dose cartridges. Each unit of issue consists of a package of 50 cartridges, organized in five blisters of ten per cardboard box. The product must be stored at controlled room temperature below 25°C (77°F), protected from light, and must not be frozen. It is regulated by the FDA and has a non-extendable shelf life of 18 months as a Type I (Code K) item. Packaging and marking must comply with Medical Marking Standard No. 1, superseding MIL-STD-129, and must ensure the product is sealed, protected from damage, and shipped in suitable commercial containers to guarantee safe delivery. Technical and quality requirements referenced in the document are governed by the DLA Master List of Technical and Quality Requirements, with revisions controlled based on solicitation or award date depending on acquisition type. This procurement is issued under Solicitation Number SPE2DP-26-T-4333 by the Department of Defense’s Medical Supply Chain Pharm FSA. One pack (PG) of 50 cartridges is required, with a delivery requirement of five days after award, delivered FOB destination to JBER, Alaska. The NSN is 6505-01-576-2767 and the purchase request number is 7017631646. The product must be supplied by an approved manufacturer with part number NDC66312-0181-16 or equivalent, and shipment must adhere to all DLA packaging standards, including commercial packaging for medical items and specific marking requirements. No quantity variance is permitted, and inspection and acceptance occur at the destination. The required delivery date is July 29, 2026, and the response deadline for the solicitation is August 3, 2026. The contracting officer must submit a referral in EBS for confirmation, including manufacturer and bidder details. Transportation and delivery logistics are governed by DLA procedural notes C19 and C20, with the point of contact for inquiries being Timothy McCauley.
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NAICS: 325412
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RINGER'S INJECTION, LACRINGER'S INJECTION, LACTATED, USP, 1000ML in packs of 12 units per case, is being procured under contract SPE2DP-26-T-4338 with a total quantity of 3 cases, each containing 12 units, for delivery to Bogalusa, LA within five days under FOB destination terms. The product must be packaged in sealed unit containers that protect against damage and shipped in commercial exterior containers suitable for safe transport by common carrier at the lowest cost, conforming to Medical Marking Standard No. 1, which supersedes MIL-STD-129. The item, manufactured by B. BROWN MEDICAL INC with NDC 00264-7750-00, has a non-extendable shelf life of 30 months and must be stored at room temperature (25°C) with brief exposure up to 40°C permitted; freezing and excessive heat must be avoided. All packaging and labeling must adhere to the latest version of the Medical Marking Standard No. 1, available through DLA Troop Support, and technical and quality requirements referenced by R or I numbers are governed by the DLA Master List in effect at the solicitation or award date. The contract specifies zero variance in quantity, inspection and acceptance occur at delivery point, and government identification must be removed from non-accepted supplies. The FDA regulates this drug, requiring buyer referral via EBS to the product specialist, including manufacturer and bidder details. The purchase is under the DoD unit of issue system, and procurement falls under NAICS 325412.
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NAICS: 325412
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EMOLLIENT LOTIONThe contract specifies the procurement of 2 bottles of Emollient Lotion, each containing 240 mL (8 FL OZ), packaged in a non-sterile bottle with a dispenser cap. The lotion must be an oil-in-water or water-in-oil emulsion containing a minimum of water, a suitable oil, an emulsifier, and a preservative, with additional compliant ingredients such as stabilizers, thickening agents, emollients, surfactants, humectants, colorants, and fragrances permitted in sufficient quantities. It must maintain a pH between 5.0 and 8.1 and exhibit a viscosity of 10,000 to 20,000 CPS at 25°C when measured with a Brookfield Viscometer Model LVT using Spindle No. 13 at 6 RPM. The product is regulated by the FDA and must be stored at controlled room temperature. Packaging and marking must comply with the latest Medical Marking Standard No. 1 and MIL-STD-129, with commercial packaging adhering to ASTM D3951 unless superseded by stricter DLA requirements. The unit of issue is a bottle (BT), and delivery is required FOB destination within 20 days of contract award to a military installation at Fort Bliss, Texas. No quantity variance is permitted, and inspection and acceptance occur at the destination. Traceable shipping methods are mandatory, and parcel post is prohibited. The contract reference number is SPE2DP-26-T-4329, with a required delivery date of July 29, 2026, and the product is identified by NSN 6508-01-019-7181. The supplier must meet all technical and quality requirements outlined in the DLA Master List of Technical and Quality Requirements.
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NAICS: 325620
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SUNSCREEN AND INSECT RThe contract specifies the procurement of a 4 oz spray bottle containing SPF 30 sunscreen and an all-natural insect repellent, packaged in units of 12 per package, with a non-extendable shelf life of 36 months as required for a Type I (Code Q) item. All packaging, marking, and labeling must comply with the Medical Marking Standard No. 1, superseding MIL-STD-129, and must ensure the product is protected from damage during transit while meeting commercial packaging standards. The item is classified as flammable/combustible, triggering adherence to Hazard Communication Standard requirements under 29 C.F.R. 1910.1200, which mandates submission of Safety Data Sheets and compliant labels prior to award, along with employee training on hazard communication protocols. The product must be delivered FOB destination within 20 days of contract award, with no tolerance for quantity variance, and must be shipped via traceable means excluding parcel post to the delivery location at Fort Bragg, North Carolina. Packaging and palletization must follow DLA’s official procurement standards, and all technical and quality requirements referenced by R or I numbers are binding as defined in the DLA Master List. The contract number is SPE2DP-26-T-4326, the NSN is 6505-01-600-3398, and the required delivery date is July 29, 2026.
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NAICS: 423450
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TOLNAFTATE CREAMTolnaftate Cream, USP, is a 1% topical antifungal cream supplied in tubes containing 15 grams each, with the unit of issue being a tube (TU). The product has a total shelf life of 36 months, and at the time of receipt by the first government activity, there must be a minimum of 31 months of remaining shelf life. It must be stored at controlled room temperature between 20-25°C (68-77°F), with short-term excursions allowed between 15-30°C (59-86°F) in accordance with USP standards. The cream is manufactured by Taro Pharmaceuticals U.S.A., Inc., with NDC 51672-2020-01, and is regulated by the FDA. All technical and quality requirements are governed by the DLA Master List of Technical and Quality Requirements, with specific references to RA001, RP001, RQ001, RS020, and RS001, which mandate compliance with FDA and DoD packaging, labeling, and shelf-life protocols. The product must be packaged in accordance with Commercial Packaging Standards as specified in the procurement document, with each unit sealed in a protective container and shipped in suitable exterior containers to ensure safe delivery via commercial carrier at the lowest rate to the designated destination. Packaging and marking must adhere strictly to Medical Marking Standard No. 1, superseding MIL-STD-129, and all labels must include required government identifiers. The shipment of 20 tubes is to be delivered FOB destination within 20 days, with no quantity variance permitted. Transportation must be via traceable means, excluding parcel post, and the item is to be delivered to the specified location in Bogalusa, Louisiana. The contract requires confirmation through EBS referral to the product specialist, ensuring proper vendor and manufacturer validation prior to award, and all documentation must comply with DLA’s acquisition and logistics directives, including palletization and hazardous material standards where applicable.
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