FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin

NDC 68788-8875 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCiprofolxacin
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208921
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (250 mg/1)
Marketing started20250519
Package count7

External sources

Source: openFDA. Public-domain (CC0).