# CHOLESTYRAMINE

NDC: 70771-1070
Generic name: CHOLESTYRAMINE
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20170608

FDA application: ANDA202902

## Active ingredients

- CHOLESTYRAMINE: 4 g/5.5g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1070"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1070
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d7c6bc5e-1916-43bf-b943-98f00f41b8de