PlainRecalls
FDA Drug Moderate Class II Ongoing

Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/ 40 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-501-30

Reported: August 20, 2025 Initiated: July 21, 2025 #D-0576-2025

Product Description

Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/ 40 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-501-30

Reason for Recall

Failed Dissolution Specifications: low dissolution results

Details

Recalling Firm
Ascend Laboratories, LLC
Units Affected
8,568 bottles
Distribution
Nationwide in the USA
Location
Bedminster, NJ

Frequently Asked Questions

What product was recalled?
Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/ 40 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-501-30. Recalled by Ascend Laboratories, LLC. Units affected: 8,568 bottles.
Why was this product recalled?
Failed Dissolution Specifications: low dissolution results
Which agency issued this recall?
This recall was issued by the FDA Drug on August 20, 2025. Severity: Moderate. Recall number: D-0576-2025.