# Ezetimibe and Simvastatin

NDC: 59651-837
Generic name: Ezetimibe and Simvastatin
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240301

FDA application: ANDA200082

## Active ingredients

- EZETIMIBE: 10 mg/1
- SIMVASTATIN: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-837"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-837
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=79dadfde-35c7-4937-9c82-1728fb6be2fb