Dried Aluminum Hydroxide Gel Tablets
» Dried Aluminum Hydroxide Gel Tablets contain not less than 90.0 percent and not more than 110.0 percent of the labeled amount of aluminum hydroxide [Al(OH)3].
Packaging and storage Preserve in well-closed containers.
Labeling Tablets may be labeled to state the aluminum hydroxide content in terms of the equivalent amount of dried aluminum hydroxide gel, on the basis that each mg of dried gel is equivalent to 0.765 mg of Al(OH)3.
A: Place a quantity of finely ground Tablets, equivalent to about 500 mg of aluminum hydroxide, in a flask equipped with a stopper and glass tubing, the tip of which is immersed in calcium hydroxide TS in a test tube. Add 5 mL of 3 N hydrochloric acid to the flask, and immediately insert the stopper: gas evolves in the flask and a precipitate is formed in the test tube.
B: The solution remaining in the flask responds to the tests for Aluminum 191.
Disintegration 701: 10 minutes, simulated gastric fluid TS being substituted for water in the test.
Uniformity of dosage units 905: meet the requirements for Weight Variation.
Acid-neutralizing capacity 301 Not less than 5 mEq of acid is consumed by the minimum single dose recommended in the labeling, and not less than 55.0% of the expected mEq value, calculated from the labeled quantity of Al(OH)3, is obtained. Each mg of Al(OH)3 has an expected acid-neutralizing capacity value of 0.0385 mEq.
Procedure Weigh and finely powder not fewer than 20 Tablets. Weigh accurately a portion of the powder, equivalent to about 1.2 g of aluminum hydroxide, add 15 mL of hydrochloric acid, and heat until dissolved. Dilute with water to about 100 mL, mix, and filter quantitatively into a 500-mL volumetric flask, washing the filter with water. Proceed as directed in the Assay under Dried Aluminum Hydroxide Gel, beginning with dilute with water to volume. Each mL of 0.05 M Edetate disodium titrant is equivalent to 3.900 mg of Al(OH)3.
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USP35NF30 Page 2133