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This Government Contract opportunity from Department Of Defense was posted on May 11, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Pharmaceutical Manufacturing and Formulation

Closed
Federal

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The contract involves the manufacture of Guaifenesin Extended-Release Tablets, 600 mg, covering all aspects from active pharmaceutical ingredient (API) sourcing and formulation to quality control and batch release testing. The work must adhere to stringent FDA and Defense Logistics Agency (DLA) standards, ensuring compliance with regulatory and military requirements. The production is intended as a subcontract and focuses on pharmaceutical manufacturing under the NAICS code 325412. The place of performance for this contract is located at Fort Stewart, with the Department of Defense’s Medical Supply Chain Pharmaceutical Field Support Activity as the overseeing agency. The contract was posted on May 11, 2026, with responses due by May 18, 2026. This opportunity provides a critical role in supplying quality-controlled and compliant pharmaceutical products to support military medical needs.

General Info

Manufacture of 600mg Guaifenesin tablets meeting FDA and DLA standards for military supply.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

NAICS

325412 - Pharmaceutical Preparation Manufacturing View NAICS

Place of Performance

FORT STEWART, GA, 31314-5185, 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 of Guaifenesin Extended-Release Tablets, 600 mg, including API sourcing, formulation, quality control, and batch release testing in compliance with FDA and DLA standards.