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This Government Contract opportunity from Department Of Defense was posted on May 28, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Pharmaceutical Manufacturing of Furosemide Injection, USP

Closed
Federal

Contract Overview

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

Active Opportunities Like This One

NAICS: 325412
New
Federal
6505--Dutasteride CapsulesThe Department of Veterans Affairs National Acquisition Center plans to issue a Request for Proposal (RFP 36E79726R0029) for the procurement of Dutasteride Capsules to serve multiple federal agencies, including the VA, Department of Defense, Bureau of Prisons, Indian Health Service, and Federal Health Care Center. This unrestricted contract aims to secure a reliable supply source for Dutasteride 0.5MG capsules in both 30-count and 90-count bottles, with annual estimated usage of approximately 3,912 and 25,502 bottles respectively. The contract will be awarded to a single responsible offeror who can provide an uninterrupted supply and will have a one-year base period followed by four one-year option periods. Distribution will be managed through the VA and DoD Pharmaceutical Prime Vendor Programs. Offerors must supply the drug under the exact name on the label, with a unique National Drug Code (NDC) exclusive to the offeror. The contractor’s label must be the sole label on the product, with VA labels designed to adhere securely on top without obscuring important information such as barcodes, expiration dates, and lot numbers. Packaging requirements include safety caps that meet specific design criteria with a minimum bottle volume of 120cc and cylindrical shape to accommodate appropriate labeling sizes. The solicitation will be released in a commercial item format in accordance with FAR Part 12 around June 22, 2026, with proposals due by July 7, 2026. Interested parties should monitor SAM.gov for updates and submit offers electronically; efforts to obtain paper copies will not be accommodated. The contract specialist and primary point of contact for this procurement is Richard Mahario.
Nac Pharmaceuticals (36E797)

POSTED

1 day ago

DEADLINE

in 20 days

AI Contract Overview

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The contract entails the manufacture and supply of sterile, preservative-free Furosemide Injection, USP, provided in 2 mL single-dose vials at a concentration of 10 mg/mL. The production must adhere to stringent standards set by the FDA, USP, and the Defense Logistics Agency (DLA), ensuring compliance with regulatory and quality requirements. The contract is a subcontract issued by the Department of Defense through the Medical Supply Chain Pharm FSA, focusing on pharmaceutical manufacturing under NAICS code 325412. The solicitation was posted on May 28, 2026, with a response deadline of June 3, 2026. The place of performance is listed as FPO with zip code 96667, and it involves supplying the product to meet federal medical supply needs. This contract seeks qualified manufacturers capable of producing high-quality sterile injections to support defense medical logistics.

General Info

Manufacture and supply sterile Furosemide Injection, 2 mL vials, FDA and DLA compliant for DoD.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

NAICS

325412 - Pharmaceutical Preparation Manufacturing View NAICS

Place of Performance

FPO, AP, 96667, US

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

PhaseClosed
Posted

subcontract

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
Office AddressN/A
ContactsNo contact information available

Full Description

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Manufacture and supply of sterile, preservative-free Furosemide Injection, USP in 2 mL single-dose vials at 10 mg/mL concentration, compliant with FDA, USP, and DLA standards.