FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin

NDC 51655-490 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208921
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20230105
Package count5

External sources

Source: openFDA. Public-domain (CC0).