A-A-0051761 (DM)
21 November 1986
INTERIM COMMERCIAL ITEM DESCRIPTION
CROMOLYN SODIUM OPHTHALMIC SOLUTION, USP
The General Services Administration has authorized the use of this Interim Commercial Item Description which was developed by DLA, Defense Personnel Support Center, Directorate of Medical Materiel, DPSC-RST, 2800 South 20th Street, Philadelphia, PA 19101, based upon currently available technical information.
Salient Characteristics:
Shall be Cromolyn Sodium Ophthalmic Solution, USP.
Shall be in accordance with the requirements of the USP.
Each milliliter of the Ophthalmicc Solution shall contain 40 mg of Cromolyn Sodium, USP (4% Ophthalmic Solution) within the applicable assay limits for the solution.
Workmanship. The solution shall be free from defects which may detract from its appearance or impair its serviceability.
Unit. Bottle (BT). One ophthalmic tip dropper bottle containing 10 ml of solution, as specified, constitutes one unit.
Contractor certification. The contractor shall certify that the product offered meets the salient characteristics of this description and conforms to the producers’ own drawings, specifications, standards, and quality assurance practices. The Government reserves the right to require proof of such conformance prior to first delivery and thereafter as may be otherwise provided for under the provisions of the contract.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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