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Lidocaine Hydrochloride and Dextrose Injection Manufacturer

Active
Federal

Contract Overview

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

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This subcontract involves the manufacture and supply of sterile, nonpyrogenic Lidocaine Hydrochloride and Dextrose Injection to support prime contractors fulfilling Department of Defense supply contracts through the Medical Supply Chain Pharm FSA. The production process requires compounding 2g of Lidocaine Hydrochloride USP and 5g of Hydrous Dextrose USP with Water for Injection USP to achieve a 500 ML bag fill volume. All manufacturing must occur in sterile compounding environments using containers that are latex-free, DEHP-free, and PVC-free to ensure full compliance with USP standards and FDA requirements. The performance of this contract is based in Williamsburg, Virginia, under NAICS code 325412. The scope of work concludes with the delivery of finished sterile injection bags. Interested parties should note the response deadline of November 3, 2026, for this specific procurement opportunity.

General Info

Manufacture and supply sterile Lidocaine and Dextrose injections for Department of Defense contracts.

NAICS

325412 - Pharmaceutical Preparation Manufacturing

Place of Performance

WILLIAMSBURG, VA, 23185-5830, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DP-27-T-0191.

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

View the prime solicitation

LIDOCAINE HYDROCHLORID

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Timeline

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA
ContactsNo contacts available
OfficeN/A
Office AddressN/A
ContactsNo contact information available

Full Description

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Manufactures and supplies sterile, nonpyrogenic Lidocaine Hydrochloride and Dextrose Injection for prime contractors delivering DLA supply contracts. Compounds 2g Lidocaine Hydrochloride USP and 5g Hydrous Dextrose USP diluted with Water for Injection USP to a 500 ML bag fill volume. Uses sterile compounding environments and latex-free, DEHP-free, and PVC-free containers. Complies with USP standards and FDA manufacturing requirements. Delivers finished sterile injection bags.

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DLA Troop Support

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