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Colesevelam

NDC 68382-619 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207765
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCOLESEVELAM HYDROCHLORIDE (625 mg/1)
Marketing started20191011
Package count3

External sources

Source: openFDA. Public-domain (CC0).