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Colesevelam Hydrochloride

NDC 43598-230 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr.Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA210889
Dosage form / routeTABLET · ORAL
Active ingredientsCOLESEVELAM HYDROCHLORIDE (625 mg/1)
Marketing started20181005
Package count1

External sources

Source: openFDA. Public-domain (CC0).