27 March 1991
COMMERCIAL ITEM DESCRIPTION
OXACILLIN SODIUM FOR ORAL SOLUTION, USP
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for Military Specification MIL-O-37467 which is cancelled.
Shall be Oxacillin Sodium for Oral Solution, USP.
Shall be in accordance with the requirements of the USP.
Shall be pleasantly-flavored, crystalline powder.
All ingredients shall be of a pharmaceutical grade.
Shall be equivalent to 250 mg of Oxacillin per 5 ml when reconstituted to 100 ml.
Workmanship. The solution shall be free from defects which detract from its appearance or impair its serviceability.
Unit. Bottle (BT). Shall be supplied as a dry mixture equivalent to 5 grams of Oxacillin in a commercially available bottle with a child-resistant safety closure and a minimum height of 51 mm base to shoulder. The bottle shall have sufficient capacity to hold 100 ml with adequate shake space. One bottle, 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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