United States · FDA National Drug Code directory
Ezetimibe
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 76333-170_161b88d8-6679-e793-e063-6394a90a481b
- Product NDC
- 76333-170
- Form
- TABLET
- Composition / generic term
- Ezetimibe
- Labeler
- Orient Pharma Co., Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220630
- Source listing expiry
- 20261231
Source-listed ingredients
- EZETIMIBE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (76333-170-12) · 76333-170-12
- 500 TABLET in 1 BOTTLE (76333-170-13) · 76333-170-13
- 90 TABLET in 1 BOTTLE (76333-170-14) · 76333-170-14
- 30 TABLET in 1 BOTTLE (76333-170-15) · 76333-170-15
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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