FDA NDC Directory · JSON-LD · Markdown

ciprofloxacin

NDC 68071-4122 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076639
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20040910
Package count6

External sources

Source: openFDA. Public-domain (CC0).