# EZETIMIBE

NDC: 31722-628
Generic name: EZETIMIBE
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220726

FDA application: ANDA210859

## 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:"31722-628"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-628
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c07fe2e0-dad4-48b5-8a07-7d57a4035ccd