Nexlizet (bempedoic acid and ezetimibe), 180ng/18mg, 30 tablets, Rx only, Manufactured for: Esperion Therapeutics, Inc, Ann Arbor, MI 48108, NDC 72426-818-03
Reported: September 13, 2023 Initiated: August 16, 2023 #D-1143-2023
Product Description
Nexlizet (bempedoic acid and ezetimibe), 180ng/18mg, 30 tablets, Rx only, Manufactured for: Esperion Therapeutics, Inc, Ann Arbor, MI 48108, NDC 72426-818-03
Reason for Recall
Failed dissolution specifications: below specification results at stability 12-month
Details
- Recalling Firm
- Esperion
- Units Affected
- 45,240 bottles
- Distribution
- Nationwide USA
- Location
- Ann Arbor, MI
Frequently Asked Questions
What product was recalled? ▼
Nexlizet (bempedoic acid and ezetimibe), 180ng/18mg, 30 tablets, Rx only, Manufactured for: Esperion Therapeutics, Inc, Ann Arbor, MI 48108, NDC 72426-818-03. Recalled by Esperion. Units affected: 45,240 bottles.
Why was this product recalled? ▼
Failed dissolution specifications: below specification results at stability 12-month
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 13, 2023. Severity: Low. Recall number: D-1143-2023.
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