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Lisinopril Tablet Manufacturing

Active
Federal

Contract Overview

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

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Nac Pharmaceuticals is seeking a subcontractor for the manufacturing of Lisinopril tablets to support Department of Veterans Affairs pharmaceutical supply projects. The selected provider will be responsible for the entire production process, including the chemical synthesis of the active pharmaceutical ingredient, formulation, compression into tablets, and rigorous quality control testing in accordance with ACS and USP-NF specifications. To qualify, the manufacturer must operate FDA-compliant cGMP facilities and possess a valid FEI number to ensure the delivery of bulk finished tablets that meet all purity and potency standards. This subcontract opportunity was posted on September 3, 2026, with a response deadline of September 24, 2026, falling under NAICS code 325412.

General Info

Nac Pharmaceuticals seeks FDA-compliant subcontractors to manufacture Lisinopril tablets for the VA.

Agency

Department Of Veterans Affairs → Nac Pharmaceuticals (36E797)View Agency

NAICS

325412 - Pharmaceutical Preparation ManufacturingView NAICS

Place of Performance

IL

Set-Aside

NONE

Documents

This scope was carved out of 36E79726R0032.

The full solicitation package (5 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

36E79726R0032 Lisinopril Tablets (VA-27-00004937)

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Veterans Affairs → Nac Pharmaceuticals (36E797)
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Veterans Affairs → Nac Pharmaceuticals (36E797)
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Office AddressN/A
ContactsNo contact information available

Full Description

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Manufactures Lisinopril tablets for prime contractors on Department of Veterans Affairs pharmaceutical supply projects. Performs chemical synthesis of the active pharmaceutical ingredient (API), formulation, compression into tablet form, and quality control testing per ACS and USP-NF specifications. Requires FDA-compliant cGMP manufacturing facilities and an FEI number. Delivers bulk finished Lisinopril tablets meeting purity and potency specifications.

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POSTED

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in 7 days
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