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sevelamer carbonate

NDC 0115-1365 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211316
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsSEVELAMER CARBONATE (800 mg/1)
Marketing started20201120
Package count1

External sources

Source: openFDA. Public-domain (CC0).