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Ciprofloxacin

NDC 80425-0492 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCiprofolxacin
Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208921
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20250202
Package count2

External sources

Source: openFDA. Public-domain (CC0).