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Pharmaceutical Supply – Cetirizine Hydrochloride Tablets

Active

Federal

Contract Overview

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

AI Contract Overview

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The contract entails the supply and delivery of 2,000 bottles of Cetirizine Hydrochloride Tablets, compliant with FDA regulations, current Good Manufacturing Practices, and Defense Logistics Agency standards. All pharmaceutical products must meet stringent quality and safety requirements, with inspections to be conducted at the destination to verify adherence to specifications. The agreement is structured as a subcontract under the NAICS code 325412, which pertains to pharmaceutical preparation manufacturing. The awarding entity is the Defense Logistics Agency, operating under the Department of Defense, and the contract was posted on August 2, 2026. Delivery and compliance are critical, with no set-aside provisions indicated, and performance is governed by the referenced DLA contract identifier SPE2D926F7855.

General Info

2,000 Cetirizine Hydrochloride tablets, FDA and DLA compliant, delivered under DLA contract SPE2D926F7855.

Agency

Department Of Defense → Defense Logistics AgencyView Agency

NAICS

325412 - Pharmaceutical Preparation ManufacturingView NAICS

Place of Performance

Not specified

Set-Aside

NONE

Documents

This scope was carved out of SPE2D926F7855.

The full solicitation package (2 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

CETIRIZINE HYDROCHLORIDE TABLETS

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Timeline

PostedAug 2

subcontract

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Organization & Contact Information

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AgencyDepartment Of Defense → Defense Logistics Agency

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Defense → Defense Logistics Agency

View Agency Profile

Office AddressN/A

ContactsNo contact information available

Full Description

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Supply and delivery of 2,000 bottles of Cetirizine Hydrochloride Tablets meeting FDA, cGMP, and DLA requirements with inspection at destination.

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