26 October 1907
INTERIM COMMERCIAL ITEM DESCRIPTION
CEFOXITIN SODIUM, STERILE, 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 of Medical Materiel, DPSC-RST, 2800 South 20th Street, Philadelphia, PA 19101, based upon currently available technical information.
Shall be Cefoxitin Sodium, Sterile, USP.
Shall be in accordance with the requirements of the USP.
All ingredients shall be of pharmaceutical grade.
For Strength 1, shall contain a quantity of Cefoxitin Sodium equivalent to 1 gram of Cefoxitin, within the applicable assay limits.
For Strength 2, shall contain a quantity of Cefoxitin Sodium equivalent to 2 grams of Cefoxitin, within the applicable assay limits.
For Strength 3, shall contain a quantity of Cefoxitin Sodium equivalent to 10 grams of Cefoxitin per bottle, within the applicable assay limits.
Strength 1, Type I and Strength 2, Type I, shall be suitable for intramuscular or intravenous use.
Strength 1 and 2, Type II, shall be suitable for intermittent intravenous administration.
Workmanship. The Products 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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