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Magnesium Sulfate

NDC 0338-1719 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameMagnesium Sulfate Heptahydrate
Labeler / ManufacturerBaxter Healthcare Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA211966
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMAGNESIUM SULFATE HEPTAHYDRATE (4 g/50mL)
Marketing started20200601
Package count1

External sources

Source: openFDA. Public-domain (CC0).