FDA NDC Directory · JSON-LD · Markdown

ciprofloxacin

NDC 43063-410 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076639
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (250 mg/1)
Marketing started20040910
Package count5

External sources

Source: openFDA. Public-domain (CC0).