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SODIUM CHLORIDE INJECT

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SPE2DP-26-T-4397Federal

Contract Overview

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

AI Contract Overview

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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.

General Info

Sodium Chloride Injection 0.9% in 1000ml bags, 12 units per package, FDA-regulated, 30-month shelf life, B. Braun sole manufacturer, FOB Carville, LA, delivery in five days.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSAView Agency

NAICS

424210 - Drugs and Druggists' Sundries Merchant WholesalersView NAICS

Place of Performance

GILLIS W LONG CENTER BLDG 13, CARVILLE, LA, 70721-0000, US

Set-Aside

NONE

Documents

(1)

SPE2DP-26-T-4397.pdf

PDF

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Timeline

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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
Timothy Mccauley
contact@example.gov
+1 (555) 000-0000

Full Description

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SODIUM CHLORIDE INJECTION
SODIUM CHLORIDE INJECTION,USP
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
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
0.9% 1000ML IV PLASTIC BAG LATEX FREE. UNIT OF ISSUE (1) PACKAGE 12's. 1 PG = 12 EA Store at 20° to 25°C (68° to 77°F) USP Controlled Room Temperature Avoid excessive heat. Protect from freezing. Store away from Incompatible Materials 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.
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/
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
SPE2DP-26-T-4397
SECTION B
RS019: Shelf-life requirement RS001 for a TYPE I (CODE P) item with a shelf life of 30 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/
B. BRAUN MEDICAL INC 11171 P/N NDC00264-5802-00 B. BRAUN MEDICAL INC 11171 P/N Q8000 ICU MEDICAL SALES, INC. 85RR5 P/N NDC00990-7983-09
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 7017684205 0001 PG 1.000
NSN/MATERIAL:6505013306269
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
SPECIAL NSN/Part Number: 6505-01-330-6269 Quantity: 1 PG Purchase Request: 7017701298QTY: 11 Delivery: 5 days ADO

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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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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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OMEPRAZOLE EXTENDED-RE
Solicitation # SPE2DP-26-T-4402
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.
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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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NAICS: 423450
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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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