# Ezetimibe

NDC: 33342-373
Generic name: Ezetimibe
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240429

FDA application: ANDA211159

## 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:"33342-373"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-373
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ebe3fa4e-82c4-4a9a-9aec-f64019391f4e