FDA NDC Directory · JSON-LD · Markdown

ciprofloxacin

NDC 85293-002 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUmasuto, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076639
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (250 mg/1)
Marketing started20250305
Package count1

External sources

Source: openFDA. Public-domain (CC0).