30 October 1991
COMMERCIAL ITEM DESCRIPTION
RIFAMPIN CAPSULES, USP
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for Military Specification MIL-R-37558 which is cancelled.
Shall be Rifampin Capsules, USP.
Shall be in accordance with the requirements of the USP.
All ingredients shall be of a pharmaceutical grade.
For Strength 1, each capsule shall contain 150 mg of Rifampin within the applicable assay limits for the capsules.
For Strength 2, each capsule shall contain 300 mg of Rifampin within the applicable assay limits for the capsules.
Each capsule 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 capsules shall be free from defects which detract from their appearance or impair their serviceability.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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