30 March 1987
INTERIM COMMERCIAL ITEM DESCRIPTION
DIETHYLPROPION HYDROCHLORIDE TABLETS, MODIFIED
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 Diethylpropion Hydrochloride Tablets, Modified.
All ingredients shall be of pharmaceutical grade.
Shall be a timed released tablet containing 75 mg of Diethylpropion Hydrochloride, within the applicable assay limits for this product.
The timed release tablets must be considered by the FDA to be therapeutically equivalent with Diethylpropion Hydrochloride Tablets, timed release, by Merrell Dow Pharmaceuticals at same dosage and administration schedule.
Workmanship. The Tablets shall be free from defects which detract from their appearance or impair their serviceability.
Unit. Bottle (BT). One bottle containing 100 tablets, as specified, constitutes one unit.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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