FDA NDC Directory · JSON-LD · Markdown

MOXIFLOXACIN HYDROCHLORIDE

NDC 71335-2329 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namemoxifloxacin hydrochloride
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA202632
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMOXIFLOXACIN HYDROCHLORIDE (400 mg/1)
Marketing started20140304
Package count2

External sources

Source: openFDA. Public-domain (CC0).