FDA NDC Directory · JSON-LD · Markdown

CIPROFLOXACIN

NDC 72189-111 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameciprofloxacin hydrochloride
Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA077859
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20200612
Marketing ended20270228
Package count4

External sources

Source: openFDA. Public-domain (CC0).