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

Pharmaceutical Packaging and Labeling Services

Closed
Federal

Contract Overview

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

Active Opportunities Like This One

NAICS: 325811
Federal
Primary Packaging of Pharmaceutical TabletsThis subcontract, issued by Nac Pharmaceuticals under the Department of Veterans Affairs, focuses on the primary packaging of Cefuroxime tablets. The scope of work requires the tablets to be packaged into either bottles or blister packs, ensuring that all final products feature compliant labeling. Essential labeling requirements include the inclusion of the lot number, expiration date, NDC code, and specific handling instructions. The project is categorized under NAICS code 325811 and was posted on December 18, 2025.
Nac Pharmaceuticals (36E797)

POSTED

11 months ago

DEADLINE

N/A

AI Contract Overview

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The contract entails secondary packaging, labeling, and boxing of transdermal patches specifically tailored to meet the stringent requirements of the Department of Veterans Affairs. Key specifications include the use of child-resistant packaging, the inclusion of only a single lot per box to ensure traceability and compliance, and adherence to standardized barcode formats for accurate inventory and distribution management. All processes must align with VA protocols to guarantee safety, consistency, and regulatory conformity across the supply chain. The work is classified as a subcontract under NAICS code 325811, indicating a focus on pharmaceutical and medicine manufacturing packaging activities. The solicitation was posted on May 11, 2026, with a response deadline set for May 18, 2026, at 6:00 PM Eastern Time. The contracting activity is managed by the National Cmop Office under the Department of Veterans Affairs, though specific placement of performance and point of contact details are not provided. Interested parties must submit proposals by the deadline to be considered, with all activities expected to fulfill federal compliance standards without exception. The scope demands precision in handling sensitive pharmaceutical products and requires proven experience with VA-specific packaging mandates.

General Info

Secondary packaging and labeling of transdermal patches with child-resistant, single-lot, barcode compliance.

Agency

Department Of Veterans Affairs → National Cmop Office (36C770)

NAICS

325811

Place of Performance

KS

Set-Aside

NONE

Documents

This scope was carved out of 36C77026Q0137.

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

View the prime solicitation

6505--CAMPHOR/MENTHOL/METHYL SALICYLATE PATCH

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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 Veterans Affairs → National Cmop Office (36C770)
ContactsNo contacts available
OfficeN/A
Organization / AgencyDepartment Of Veterans Affairs → National Cmop Office (36C770)
Office AddressN/A
ContactsNo contact information available

Full Description

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Secondary packaging, labeling, and boxing of transdermal patches to meet VA requirements including child-resistant packaging, single-lot-per-box, and barcode standards.

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DEADLINE

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NAICS: 325412
New
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SOURCES SOUGHT Charleston CMOP CARBOXYMETHYLCELLULOSE NA 0.25% OPH SOLN 15ML
Solicitation # 36C77027Q0019
The Department of Veterans Affairs, through the National CMOP Office, is conducting a sources sought market research effort under solicitation 36C77027Q0019 for Carboxymethylcellulose NA 0.25% Ophthalmic Solution 15ML. This effort is intended to identify capable vendors for the Charleston CMOP in South Carolina. Interested parties must submit responses via email to Sarah Fry, providing their business size, classification, and UEI number, along with a confirmation of whether they possess direct Original Equipment Manufacturer (OEM) documentation to prevent gray market and counterfeit items. Technical requirements specify that products must have an FDA therapeutic equivalence code of A, unless all drugs in the family group are B rated, and must comply with the Drug Supply Chain Security Act. Deliveries are expected 10 days after receipt of order, with pharmaceutical expiration dates required to be at least 12 months from the delivery date. Packaging must adhere to strict standards, including the use of child-proof caps for packages under 500 count and specific bottle dimensions. Furthermore, all products must feature unit-of-use bar coding conforming to GS1-128, HIBCC, or HIBC standards with a minimum of ANSI/ISO/IEC Quality Grade C. All shipments must include detailed packing slips containing the VA purchase order and obligation numbers, NDC, and product line-item numbers.
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