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Cholestyramine

NDC 68094-906 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerPrecision Dose, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209599
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsCHOLESTYRAMINE (4 g/4.8g)
Marketing started20231215
Package count2

External sources

Source: openFDA. Public-domain (CC0).