# Ezetimibe

NDC: 71205-145
Generic name: Ezetimibe
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170612

FDA application: ANDA203931

## Active ingredients

- EZETIMIBE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-145"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-145
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5cbd9bce-e02d-440f-95d5-4eb958d2f4f3