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zinc sulfate

NDC 70710-1877 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic namezinc sulfate injection,
Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217074
Dosage form / routeSOLUTION · INTRAVENOUS
Active ingredientsZINC SULFATE (3 mg/mL)
Marketing started20231207
Package count1

External sources

Source: openFDA. Public-domain (CC0).