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Colesevelam Hydrochloride

NDC 33342-197 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204893
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCOLESEVELAM HYDROCHLORIDE (625 mg/1)
Marketing started20250418
Package count1

External sources

Source: openFDA. Public-domain (CC0).