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Ciprofloxacin

NDC 51655-216 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameCiprofloxacin Hydrochloride
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077859
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20230317
Marketing ended20270228
Package count6

External sources

Source: openFDA. Public-domain (CC0).