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SEVELAMER CARBONATE

NDC 58624-5001 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerShandong Xinhua Pharmaceutical Co., Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA215998
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSEVELAMER CARBONATE (800 mg/1)
Marketing started20250227
Package count2

External sources

Source: openFDA. Public-domain (CC0).