20 April 1990
COMMERCIAL ITEM DESCRIPTION
IMIPRAMINE HYDROCHLORIDE TABLETS, USP
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for Military Specification MIL-I-37752 which is cancelled.
Shall be Imipramine Hydrochloride Tablets, USP.
Shall be in accordance with the requirements of the USP.
All ingredients shall be of a pharmaceutical grade.
For Strength 1, shall contain 25 mg of Imipramine Hydrochloride per tablet within the applicable assay limits for the tablets.
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. Bottle (BT).
For Size – I. One bottle containing 100 tablets, as specified, constitutes one unit.
For Size – II. One bottle containing 1000 tablets, as specified, constitutes one unit.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
For Parts Inquires submit RFQ to Parts Hangar, Inc.
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