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Moxifloxacin

NDC 63323-850 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameMOXIFLOXACIN HYDROCHLORIDE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryNew Drug Application (innovator) · App NDA205572
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMOXIFLOXACIN HYDROCHLORIDE (400 mg/250mL)
Marketing started20150318
Package count1

External sources

Source: openFDA. Public-domain (CC0).