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Moxifloxacin

NDC 68180-422 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202867
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsMOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE (5 mg/mL)
Marketing started20170701
Package count1

External sources

Source: openFDA. Public-domain (CC0).