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This Subcontract opportunity from Department Of Defense was posted on August 30, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Manufacture and Supply of Dextrose Injection 5%, USP

Closed
Federal

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This subcontract involves the manufacture and supply of sterile Dextrose Injection 5% for prime contractors supporting the Defense Logistics Agency medical supply chain. The scope of work includes compounding Hydrous Dextrose USP with Water for Injection USP, filling 1,000 ML containers, and performing sterilization and quality testing to ensure full USP compliance. All production must occur within an FDA-approved facility using pharmaceutical-grade equipment. The contractor is responsible for delivering finished, packaged containers that adhere to DLA RP001 packaging standards. This requirement falls under NAICS code 325412 and is managed by the Department of Defense Medical Supply Chain Pharm FSA. The performance location is designated as FPO 09592-1200, with a response deadline of September 8, 2026.

General Info

Manufacture and supply sterile Dextrose Injection 5% for DLA by September 8, 2026.

NAICS

325412 - Pharmaceutical Preparation Manufacturing

Place of Performance

FPO, AE, 09592-1200, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DP-26-T-4789.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

DEXTROSE INJECTION,

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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
Office AddressN/A
ContactsNo contact information available

Full Description

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Manufactures and supplies sterile Dextrose Injection 5% for prime contractors on Defense Logistics Agency (DLA) medical supply contracts. Compounds Hydrous Dextrose USP with Water for Injection USP, performs sterilization and filling of 1,000 ML containers, and conducts quality testing for USP compliance. Uses pharmaceutical-grade mixing and sterilization equipment. Requires FDA-approved facility and DLA RP001 packaging compliance. Delivers finished, packaged containers.

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