FDA NDC Directory · JSON-LD · Markdown

Cholestyramine

NDC 63629-2162 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Generic namecholestyramine
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA077203
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCHOLESTYRAMINE (4 g/5g)
Marketing started20050915
Package count1

External sources

Source: openFDA. Public-domain (CC0).