# Ezetimibe

NDC: 10135-787
Generic name: Ezetimibe
Labeler / Manufacturer: Marlex Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240101

FDA application: ANDA215693

## Active ingredients

- EZETIMIBE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"10135-787"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10135-787
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=109a22f4-a7cb-96c6-e063-6394a90ad7f6