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This Government Contract opportunity from Department Of Defense was posted on May 17, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Pharmaceutical Manufacturing and Fill-Finish Services

Closed
Federal

Contract Overview

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The contract involves the manufacturing and fill-finish services for Maropitant Citrate at a concentration of 10mg/mL, packaged in 20mL vials. The scope covers the full process from formulation through sterile filling, capping, and comprehensive batch testing, all conducted under current Good Manufacturing Practice (cGMP) standards to ensure quality and compliance. This subcontract falls under the pharmaceutical manufacturing sector, specifically NAICS code 325412. The work is solicited by the Department of Defense's Medical Supply Chain Pharmaceutical FSA, with performance located in San Antonio, Texas (ZIP code 78226). The contract timeline includes a solicitation posting date of May 17, 2026, with proposals due by May 26, 2026. This contract supports the Department of Defense’s supply chain needs for pharmaceutical products requiring stringent sterile processing and quality assurance.

General Info

Manufacturing and fill-finish of Maropitant Citrate 10mg/mL sterile vials under cGMP for DoD.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

NAICS

325412 - Pharmaceutical Preparation Manufacturing View NAICS

Place of Performance

SAN ANTONIO, TX, 78226, 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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Contract manufacturing of Maropitant Citrate 10mg/mL in 20mL vials, including formulation, sterile filling, capping, and batch testing under cGMP conditions.