FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin

NDC 82804-130 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCiprofolxacin
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA208921
Dosage form / routeTABLET · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20231001
Package count5

External sources

Source: openFDA. Public-domain (CC0).