FDA NDC Directory · JSON-LD · Markdown

Cipro

NDC 50419-754 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameciprofloxacin hydrochloride
Labeler / ManufacturerBayer HealthCare Pharmaceuticals Inc.
Marketing categoryNew Drug Application (innovator) · App NDA019537
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started19871022
Package count1

External sources

Source: openFDA. Public-domain (CC0).