18 December 1992
COMMERCIAL ITEM DESCRIPTION
CEFADROXIL CAPSULES, USP
The General Services Administration has authorized the use of this Commercial Item Description.
Shall be Cefadroxil Capsules, USP.
Shall be in accordance with the requirements of the USP.
All ingredients shall be of a pharmaceutical grade.
Shall contain a sufficient amount of Cefadroxil Monohydrate equivalent to 500 mg of Cefadroxil in each capsule within the applicable assay limits for the capsules.
Each capsule shall be marked/embossed with a product identification code to identity the active ingredient(s), strength, and manufacturer. The materials used in marking/embossing the dosage forms shall be acceptable to the FDA. The actual code used for the product shall be left to the discretion of the supplier.
Workmanship. The capsules shall be free from defects which detract from their appearance or impair their serviceability.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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