# Ezetimibe

NDC: 76333-170
Generic name: Ezetimibe
Labeler / Manufacturer: Orient Pharma Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220630

FDA application: ANDA215693

## 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:"76333-170"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76333-170
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b6e77d9b-a553-63e0-e053-2a95a90a18fe