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sevelamer hydrochloride

NDC 68462-447 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA204724
Dosage form / routeTABLET, FILM COATED · PARENTERAL
Active ingredientsSEVELAMER HYDROCHLORIDE (800 mg/1)
Marketing started20190208
Package count2

External sources

Source: openFDA. Public-domain (CC0).