United States · FDA National Drug Code directory

Nexlizet

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
72426-818_29da37de-60f3-4dcc-8ccd-1b96631778bd
Product NDC
72426-818
Form
TABLET, FILM COATED
Composition / generic term
Bempedoic Acid and Ezetimibe
Labeler
Esperion Therapeutics, Inc.
Marketing category
NDA
Marketing start / end (source format)
20200309
Source listing expiry
20271231

Source-listed ingredients

  • BEMPEDOIC ACID — 180 mg/1
  • EZETIMIBE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72426-818-03) · 72426-818-03
  • 7 TABLET, FILM COATED in 1 BLISTER PACK (72426-818-99) · 72426-818-99

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.

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Nexlizet — United States | Molindra Medicines