FDA NDC Directory · JSON-LD · Markdown

sodium sulfate, potassium sulfate, and magnesium sulfate

NDC 69452-428 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerBionpharma Inc.,
Marketing categoryAbbreviated NDA (generic) · App ANDA204135
Dosage form / routeSOLUTION · ORAL
Active ingredientsMAGNESIUM SULFATE ANHYDROUS (1.6 g/177mL)
POTASSIUM SULFATE (3.13 g/177mL)
SODIUM SULFATE (17.5 g/177mL)
Marketing started20250415
Package count1

External sources

Source: openFDA. Public-domain (CC0).