FDA NDC Directory · JSON-LD · Markdown

Ciprofloxacin Hydrochloride

NDC 83939-0002 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerVERITYRX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076593
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCIPROFLOXACIN HYDROCHLORIDE (500 mg/1)
Marketing started20240523
Package count3

External sources

Source: openFDA. Public-domain (CC0).