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Ciprofloxacin

NDC 70934-965 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameCiprofloxacin Hydrochloride
Labeler / ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA076126
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20220502
Marketing ended20260831
Package count5

External sources

Source: openFDA. Public-domain (CC0).