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Pharmaceutical Supply – Guaifenesin Extended Release (NSN 6505017249533)

Active

Federal

Contract Overview

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

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The contract entails the supply and delivery of 25 units of Guaifenesin Extended Release, identified by NSN 6505017249533, to Fort Bragg, North Carolina. The product must strictly comply with FDA regulations, and no substitutions or alternative formulations are permitted under any circumstances. This is a subcontract issued under the Department of Defense through the Defense Logistics Agency, with the North American Industry Classification System code 325412 indicating pharmaceutical manufacturing. The solicitation was posted on July 20, 2026, and the delivery is to be fulfilled under contract SPE2DP26F7786, specifically tied to award SPE2DX25D9900. All terms require adherence to federal pharmaceutical standards and the designated delivery location, with no flexibility in product specification or sourcing.

General Info

Supply 25 units Guaifenesin ER to Fort Bragg under DOD contract, no substitutions, FDA-compliant only.

Agency

Department Of Defense → Defense Logistics AgencyView Agency

NAICS

325412 - Pharmaceutical Preparation ManufacturingView NAICS

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of SPE2DP26F7786.

The full solicitation package (2 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

GUAIFENESIN EXTENDE

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Timeline

PostedJul 20

subcontract

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Organization & Contact Information

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AgencyDepartment Of Defense → Defense Logistics Agency

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Defense → Defense Logistics Agency

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Office AddressN/A

ContactsNo contact information available

Full Description

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Supply and delivery of 25 units of Guaifenesin Extended Release conforming to NSN 6505017249533 for delivery to Fort Bragg, NC. Product must be FDA-compliant with no substitutions allowed.

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