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Colesevelam Hydrochloride

NDC 68462-620 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerGlenmark Pharmaceuticals Inc.,USA
Marketing categoryAbbreviated NDA (generic) · App ANDA202190
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCOLESEVELAM HYDROCHLORIDE (3.75 g/1)
Marketing started20180716
Package count1

External sources

Source: openFDA. Public-domain (CC0).