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Sodium Sulfate, Potassium Sulfate and Magnesium Sulfate

NDC 67877-725 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213924
Dosage form / routeSOLUTION · ORAL
Active ingredientsMAGNESIUM SULFATE, UNSPECIFIED FORM (1.6 g/177mL)
POTASSIUM SULFATE (3.13 g/177mL)
SODIUM SULFATE (17.5 g/177mL)
Marketing started20240329
Package count1

External sources

Source: openFDA. Public-domain (CC0).