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ciprofloxacin

NDC 54348-663 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCIPROFLOXACIN
Labeler / ManufacturerPharmPak, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076639
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20190710
Package count3

External sources

Source: openFDA. Public-domain (CC0).