# Ezetimibe

NDC: 51660-200
Generic name: Ezetimibe
Labeler / Manufacturer: Ohm Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170612

FDA application: ANDA207311

## 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:"51660-200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51660-200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5b3842f6-c80a-47b8-8a82-b69e465b05f7