21 July 1987
COMMERCIAL ITEM DESCRIPTION
AMANTADINE HYDROCHLORIDE CAPSULES, USP
The General Services Administration has authorized the use of this Commercial Item Description.
Shall be Amantadine Hydrochloride Capsules, USP.
Shall be in accordance with the requirements of the USP.
All ingredients shall be of pharmaceutical grade.
Shall contain 100 mg of Amantadine Hydrochloride per capsule within the applicxable assay limits for the capsules.
Workmanship. The Capsules shall be free from defects which detract their appearance or impair their serviceability.
For Size 1 – Bottle (BT). One bottle containing 100 capsules, as specified, constitutes one unit.
For Size 2 – Bottle (BT). One bottle containing 500 capsules, as specified, constitutes one unit.
For Size 1 – Pakcage (PG). One package containing 100 individually sealed capsules (unit dose), as specified, constitutes one unit.
Contractor certification. The contractor shall certify that the product offered meets the salient characteristics of this description and conforms to the producers’ own drawings, specifications, standards, and quality assurance practices. The Government reserves the right to require proof of such conformance prior to first delivery and thereafter as may be otherwise provided for under the provisions of the contract.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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