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This Subcontract opportunity from Department Of Defense was posted on July 13, 2026. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Supply of Valsartan/Hydrochlorothiazide 160-12.5 mg Tablets (90-count bottles)

Closed
Federal

Contract Overview

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NAICS: 325412
New
Federal
6505--Request for Information (RFI) - Specialty – PPV 2028 Amendment 0002 to Extend Response Date from Nov. 16, 2026 to Nov. 30, 2026 at 11AM CT
Solicitation # 36E79727Q0001
The Department of Veterans Affairs, through the OALC Enterprise Procurement Office, has issued a Request for Information regarding the Pharmaceutical Prime Vendor (PPV) 2028 program. The agency is seeking market research to determine the feasibility of integrating Limited Distribution and Closed Distribution Products (CDP) into the PPV scope. These specialty medications are typically high-cost, low-volume items with restricted distribution channels that often require specific clinical justifications, manufacturer-mandated registrations, and specialized safety monitoring. The primary objective is to establish a seamless ordering platform where all Federal Supply Schedule (FSS) items, including those that bypass the physical possession of the prime vendor, are visible and orderable with accurate invoicing and delivery tracking for VA medical centers nationwide. The government is soliciting detailed feedback from industry partners on their ability to coordinate fulfillment with manufacturer-designated specialty distributors and their capacity to provide consistent reporting and reconciliation for these transactions. Potential respondents must provide their company name, point of contact information, UEI, CAGE code, and any applicable socioeconomic designations. Submissions are due by 11 AM Central on November 16, 2026, via email to Karen Ade. This notice is strictly for market research purposes and does not constitute a formal solicitation or a commitment by the government to award a contract.
Nac Prime Vendor (36W797)

POSTED

about 19 hours ago

DEADLINE

in 20 days

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The contract requires the manufacture, labeling, packaging, and delivery of FDA-approved generic Valsartan/Hydrochlorothiazide 160-12.5 mg tablets in 90-count bottles, fully compliant with current good manufacturing practices, the Drug Supply Chain Security Act, and all federal labeling requirements. Production must include precise barcoding to ensure compatibility with automated dispensing systems and adherence to quarterly reporting obligations for regulatory and inventory tracking purposes. The product must meet all pharmaceutical quality benchmarks and be distributed under strict regulatory oversight to ensure patient safety and supply chain integrity. This subcontract is issued by the Department of Defense through DLA Troop Support, with a posted date of July 13, 2026, and a response deadline of August 13, 2026. The NAICS code 325412 confirms the activity falls under pharmaceutical and medicine manufacturing. There is no designated set-aside classification, and performance location details are unspecified, though the end-use is tied to federal healthcare logistics. All work must be completed in accordance with federal procurement and pharmaceutical standards, with no deviations permitted in formulation, labeling, or packaging protocols.

General Info

Manufacture and deliver FDA-approved Valsartan/Hydrochlorothiazide 160-12.5 mg tablets in 90-count bottles under strict federal pharmaceutical and DLA regulations.

NAICS

325412 - Pharmaceutical Preparation Manufacturing

Place of Performance

PA

Set-Aside

NONE

Documents

0

No documents available

Documents will appear here when they are available.

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Uniform Contract Format

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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 → DLA Troop Support
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Manufacture, label, package, and deliver FDA-approved generic pharmaceuticals in compliance with cGMP, DSCSA, and federal labeling standards. Includes quarterly reporting and barcoding for automated dispensing systems.

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