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
50090-7339_27b6d944-b73a-4d09-9562-ef8f02f49d31
Product NDC
50090-7339
Form
TABLET
Composition / generic term
Ezetimibe
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20220429
Source listing expiry
20261231

Source-listed ingredients

  • EZETIMIBE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (50090-7339-0) · 50090-7339-0
  • 90 TABLET in 1 BOTTLE (50090-7339-1) · 50090-7339-1

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →