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This document provides information on levofloxacin tablets, including identification tests, assays, and dissolution tests. It defines levofloxacin tablets as containing between 90-110% of the labeled amount of levofloxacin. The identification tests match retention times and UV spectra of samples to standards. The assay uses HPLC to determine the levofloxacin amount is within limits. Two dissolution tests are described using UV analysis to show at least 80% or amounts in Table 1 are dissolved within 30 minut

Author

grace_febianty

Language

EN