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ciprofloxacin

NDC 42708-192 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerQPharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076639
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20040910
Package count1

External sources

Source: openFDA. Public-domain (CC0).