# CHOLESTYRAMINE LIGHT

NDC: 24658-271
Generic name: cholestyramine light
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: ANDA074558

## Active ingredients

- CHOLESTYRAMINE: 4 g/5.7g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24658-271"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24658-271
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=31655681-125c-4eaa-959b-8f434bb43590