FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin

NDC 71335-2097 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA208921
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (250 mg/1)
Marketing started20200812
Package count10

External sources

Source: openFDA. Public-domain (CC0).