FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin

NDC 71205-997 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameCiprofloxacin Hydrochloride
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA076126
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20091010
Package count6

External sources

Source: openFDA. Public-domain (CC0).