11 June 1987
30 July 1986
COMMERCIAL ITEM DESCRIPTION
TIMOLOL MALEATE OPTHALMIC SOLUTION, USP
The General Services Administration has authorized the use of this Commercial Item Description.
Shall be Timolol Maleate Opthalmic Solution, USP.
Shall be in accordance with the requirements of the USP.
Materials used in manufacture shall be of pharmaceutical grade.
For Strength 1, shall be a sterile, isotonic, buffered, aqueous, ophthalmic solution containing the equivalent of 0.25% of Timolol, within the applicable assay limits for the solution.
For Strength 2, shall be a sterile, isotonic, buffered, aqueous, ophthalmic containing the equivalent of 0.5% of Timolol, 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).
For Size 1, one commercially available ophthalmic dropper-tip squeeze bottle containing 5 ml, as specified, constitutes one unit.
For Size 2, one commercially available ophthalmic dropper tip squeeze bottle containing 10 ml, as specified, constitutes one unit.
DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited.
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