# CHOLESTYRAMINE

NDC: 68382-528
Generic name: CHOLESTYRAMINE
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20180801

FDA application: ANDA202901

## Active ingredients

- CHOLESTYRAMINE: 4 g/9g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68382-528"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-528
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=acc48703-c15b-4275-aa75-749f1c07dcbb