Ascend Laboratories, Llc: Amlodipine And Olmesartan Medoxomil Tablets, 10 Mg/20 Mg, 30 Tablets Per Bottle
Recall Summary Ascend Laboratories is recalling Amlodipine and Olmesartan Medoxomil Tablets (10 mg/20 mg) in 30-tablet bottles nationwide because the tablets don't dissolve properly and contain less olmesartan than specified. This combination medication is used to treat high blood pressure. The recall affects bottles distributed across all U.S. states and Washington, D.C.
- Recalling firm
- Ascend Laboratories, LLC
- Product
- Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg, 30 Tablets per bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC., Parsnippany, NJ 07054. NDC: 67877-500-30
- Reason
- Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-07-08
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide in the USA
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/5e5011cc-1c0c-4435-a131-e8b7ba3ccb57