NDC 72426-818 – Nexlizet

Bempedoic Acid 180 mg/1; Ezetimibe 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 2 recalls

Product NDC72426-818

Product details

Brand name
Nexlizet
Generic name
Bempedoic Acid and Ezetimibe
Labeler
Esperion Therapeutics, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA211617
Marketed since
March 9, 2020
Listing expires
December 31, 2027
Pharmacologic class
Adenosine Triphosphate-Citrate Lyase Inhibitor; Dietary Cholesterol Absorption Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Nexlizet →

Package NDC codes (2)

Package NDCDescriptionSince
72426-818-0330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72426-818-03)Mar 9, 2020
72426-818-99 sample7 TABLET, FILM COATED in 1 BLISTER PACK (72426-818-99)Mar 9, 2020

Recalls mentioning this NDC