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Ciprofloxacin

NDC 58657-676 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerMethod Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208921
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20200812
Package count1

External sources

Source: openFDA. Public-domain (CC0).