30 November 1990
COMMERCIAL ITEM DESCRIPTION
DIGOXIN ELIXIR, USP
The General Services Administration has authorized the use of this Commercial Item Description as a replacement for Military Specification MIL-D-36238B which is cancelled.
Shall be pleasantly flavored Digoxin Elixir, USP, suitable for pediatric use.
Shall be in accordance with the requirements of the USP.
All ingredients shall be of a pharmaceutical grade.
Shall contain 0.05 mg of Digoxin in each ml of elixir, within the applicable assay limits for the elixir.
Shall be supplied 60 ml in a commercially available bottle, packaged together with a separate medicine dropper to constitute the unit. The dropper shall be accurately calibrated from 0.4 ml to 1.0 ml intervals. Main (bold) graduation marks shall be at 0.4, 0.6, 0.8, and 1.0 ml with the appropriate numbers.
Workmanship. The elixir shall be free from defects which detract from its appearance or impair its serviceability. †††††††††††
Unit. Package (PG). One package containing one bottle and dropper,† 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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