A-A-54455
Each tablet shall be marked/embossed with a product identification code to identify 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 tablets shall be free from defects which detract from their appearance or impair their serviceability.
Unit.
For Size 1 – Bottle (BT). One bottle containing 50 tablets, as specified, constitutes one unit.
For Size 2 – Bottle (BT). One bottle containing 100 tablets, as specified, constitutes one unit.
For Size 3 – Bottle (BT). One bottle containing 500 tablets, as specified, constitutes one unit.
For Size 4 – Bottle (BT). One bottle containing 1000 tablets, as specified, constitutes one unit.
For Size 5 – Package (PG). One package containing 100 tablets individually sealed in a blister or strip package of 10 tablets for unit dose, as specified, constitutes one unit.
For Size 6 – Package (PG). One package containing 21 tablets for a 6 day drug therapy regimen, 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.
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