30 August 1993
10 October 1988
COMMERCIAL ITEM DESCRIPTION
ACEBUTOLOL HYDROCHLORIDE CAPSULES
The General Services Administration has authorized the use of this Commercial Item Description.
Shall be Acebutolol Hydrochloride Capsules.
All ingredients shall be of a pharmaceutical grade.
For Strength 1, shall contain Acebutolol Hydrochloride equivalent to 200 mg Acebutolol per capsule, within the applicable assay limits.
For Strength 2, shall contain Acebutolol Hydrochloride equivalent to 400 mg Acebutolol per capsule, within the applicable assay limits.
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.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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