31 August 1990
COMMERCIAL ITEM DESCRIPTION
IRON DEXTRAN INJECTION, USP
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for Military Specification MIL-I-37912 which is cancelled.
Shall be Iron Dextran Injection, USP.
Shall be in accordance with the requirements of the USP.
All ingredients shall be of a pharmaceutical grade.
Shall be suitable for intramuscular use.
Shall contain a quantity of Iron Dextran, equivalent to 50 mg per ml of elemental iron within the applicable assay limits.
Workmanship. The product shall be free from defect which detract from its appearance or impair its serviceability.
For Size 1. Package (PG). Shall be supplied 10 ml in a bottle. One package containing two (2) bottles, as specified, constitutes one unit.
For Size 2. Vial (VI). One vial containing ten 10 ml, 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 producersí 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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