28 April 1987
INTERIM COMMERCIAL ITEM DESCRIPTION
AMPICILLIN FOR ORAL SUSPENSION, USP
The General Services Administration has authorized the use of this Interim Commercial Item Description which was developed by the Defense Personnel Support Center, Directorate of Medical Materiel, DPSC-RST, 2800 South 20th Street, Philadelphia, PA 19101, based upon currently available technical information.
Shall be palatable Ampicillin for Oral Suspension, USP.
Shall be in accordance with the requirements of the USP.
Materials used in the manufacture of the product shall be of a pharmaceutical grade.
For Strength 1, shall contain a quantity of ampicillin (anhydrous or as the trihydrate), equivalent to 125 mg Ampicillin per 5 ml, within the applicable assay limits.
For Strength 2, shall contain a quantity of ampicillin (anhydrous or as the the trihydrate), equivalent to 250 mg Ampicillin per 5 ml, within the applicable assay limits.
Workmanship. The Product shall be free from defects which detract from its appearance or impair its serviceability.
Unit. Bottle (BT).
For Size 1, shall be supplied as a dry mixture, equivalent to 5 grams of Ampicillin (125 mg per 5 ml when reconstituted to 200 ml), in a bottle (minimum height 51 mm base to shoulder) with child-resistant safety closure and sufficient capacity to hold 200 ml with adequate space. one bottle, as specified, constitutes one unit.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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