Manufacture of solid dosage forms, the rate active pharma ingredient is dissolved simulating the digestive tract fluids is determined with dissolution testing.

Dissolution tests are commonly conducted to check the time taken for the active ingredient in a dosage form to release into the body and help predict how the drug performs inside the body.

Jubilant Cadista Pharmaceuticals Inc. Issues Voluntary Nationwide Recall of Drospirenone and Ethinyl Estradiol Tablets, USP, Due to Out-of-Specification Dissolution Test Results ...