FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin

NDC 71335-1347 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameCiprofloxacin Hydrochloride
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA076126
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20091010
Package count10

External sources

Source: openFDA. Public-domain (CC0).