FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin

NDC 67296-2135 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCiprofolxacin
Labeler / ManufacturerRedpharm Drug
Marketing categoryAbbreviated NDA (generic) · App ANDA208921
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20231001
Package count4

External sources

Source: openFDA. Public-domain (CC0).