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COLESTIPOL HYDROCHLORIDE

NDC 0115-5211 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077510
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCOLESTIPOL HYDROCHLORIDE (1 g/1)
Marketing started20210817
Package count2

External sources

Source: openFDA. Public-domain (CC0).