# CHOLESTYRAMINE

NDC: 24658-266
Generic name: cholestyramine
Labeler / Manufacturer: PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20230314

FDA application: ANDA074557

## Active ingredients

- CHOLESTYRAMINE: 4 g/9g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24658-266"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24658-266
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d82647da-465b-4e2e-8cf8-72d50f047b3e