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METRONIDAZOLE

NDC 47335-993 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namemetronidazole
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212435
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMETRONIDAZOLE (500 mg/100mL)
Marketing started20210810
Package count1

External sources

Source: openFDA. Public-domain (CC0).