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CHOLESTYRAMINE LIGHT

NDC 24658-270 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Generic namecholestyramine light
Labeler / ManufacturerPURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
Marketing categoryAbbreviated NDA (generic) · App ANDA074558
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCHOLESTYRAMINE (4 g/5.7g)
Marketing started20230314
Package count1

External sources

Source: openFDA. Public-domain (CC0).