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This document describes a study comparing the dissolution of generic ciprofloxacin tablets to innovator ciprofloxacin tablets. The study used a dissolution test with pH buffers of 1.2, 4.5, and 6.8 to test the tablets. Dissolution results were analyzed using high performance liquid chromatography. Based on f1 and f2 values, the generic tablets met equivalence criteria compared to the innovator tablets in all pH buffers, indicating they are equivalent in vitro. The study aimed to provide evidence of generic

Author

yudhit bessie

Language

EN