FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin

NDC 70518-4133 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCiprofolxacin
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA208921
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (250 mg/1)
Marketing started20240703
Package count4

External sources

Source: openFDA. Public-domain (CC0).