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Moxifloxacin Hydrochloride

NDC 57237-156 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202632
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMOXIFLOXACIN HYDROCHLORIDE (400 mg/1)
Marketing started20140304
Package count1

External sources

Source: openFDA. Public-domain (CC0).