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Azelastine Hydrochloride Nasal Solution Manufacturer

Active

Federal

Response Deadline11/02/2026, 05:00:00 PM UTC

Contract Overview

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

AI Contract Overview

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This subcontract involves the manufacture and supply of Azelastine Hydrochloride Nasal Solution 0.1% for prime contractors supporting Department of Defense DLA Troop Support Medical Supply Chain projects. The selected manufacturer is responsible for producing 30,000 bottles of the drug formulation within FDA and cGMP compliant facilities, ensuring strict adherence to the DLA Master List of Technical and Quality Requirements and Medical Marking Standard No. 1. The project falls under NAICS code 325412 and is managed by the Medical Supply Chain Pharm FSA. Interested parties must note the response deadline of November 2, 2026, to provide the required pharmaceutical products according to the specified technical standards.

General Info

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

NAICS

325412 - Pharmaceutical Preparation Manufacturing

Place of Performance

DEU

Set-Aside

NONE

Documents

This scope was carved out of SPE2DP-27-T-0160.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

AZELASTINE HYDROCHLORI

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Timeline

PostedOct 25

subcontract

Response DeadlineNov 2

Submission deadline

Response Deadline

11/02/2026, 05:00:00 PM UTCin 8 days

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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 / AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

Office AddressN/A

ContactsNo contact information available

Full Description

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Supplies finished pharmaceutical product for prime contractors on DLA Troop Support Medical Supply Chain projects. Manufactures Azelastine Hydrochloride Nasal Solution 0.1% (137 mcg per spray) in bottle format using FDA/cGMP compliant facilities. Adheres to DLA Master List of Technical and Quality Requirements (RA001) and Medical Marking Standard No. 1. Delivers 30,000 bottles of the approved drug formulation.

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