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Sevelamer Hydrochloride

NDC 70710-2058 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218966
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSEVELAMER HYDROCHLORIDE (800 mg/1)
Marketing started20250301
Package count1

External sources

Source: openFDA. Public-domain (CC0).