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MAGNESIUM SULFATE

NDC 47335-992 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namemagnesium sulfate heptahydrate
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213917
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMAGNESIUM SULFATE HEPTAHYDRATE (40 mg/mL)
Marketing started20210801
Package count2

External sources

Source: openFDA. Public-domain (CC0).