DOD A-A-0053359-1988 HYDROCORTISONE ACETATE USP《美国标准氢化可的松醋酸盐》.pdf
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1、A-A-O053359 (DM) 14 February 1988 INTERIM COMMERCIAL ITEM DESCRIPTION HYDROCORTISONE ACETATE, USP The General Services Administration has authorized the use of this Interim Commercial Item Description which was developed by the Defense Personnel Support Center, Directorate ofMedica1 Materiel, DPSC-R
2、ST, 2800 South 20th Street, Philadelphia, PA 19101, based upon currently available technical information. Salient characteristics: Shall be Hydrocortisone Acetate, USP, in powder form. A-A-0053359 65 W 99799Li 00303bl O = C- 625- - 05 Shall be in accordance with the requirements of the USP. Shall be
3、 suitable for use in pharmaceutical compounding. All ingredients shall be of pharmaceutical grade. Workmanship. The powder shall be free from defects which detract from its appearance or impair its serviceability. Unit. Bottle (BT). One bottle containing 100 grams, as specified, constitutes one unit
4、. 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 c
5、onformance prior to first delivery and thereafter as may be otherwise provided for under the provisions of the contract. Regulatory requirements. Federal Food, Drug and Cosmetic Act. If the product covered by this document has been determined by the U.S. Food and Drug Administration to be under its
6、jurisdiction, the offeror/contractor shall comply, and be responsible for compliance by its subcontractors/supplers, with the requirements AMSC/NA FSC 6505 DISTRIBUTION STATEMENT A. Approved for public release: distribution is unlimited. 0 K THIS DOCUMENT CONTAINS 2 . PAGES. Provided by IHSNot for R
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