Drug recall D-0237-2024
Product
Ibuprofen and Famotidine Tablets 800mg/26.6mg, Rx Only, 90 Tablets per Bottle, manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories, LLC., Parsippany, NJ 07054, NDC 67877-626-90
Reason for recall
Presence of Foreign Tablet/Capsule: A stray Rasagiline Mesylate 1 mg tablet was discovered in an unopened bottle of Ibuprofen and Famotidine.
Lots and codes
23140190, Exp. Date 12/31/2024
Recall details
- Recalling firm
- Ascend Laboratories, LLC, Parsippany, NJ
- Quantity
- 3,288 bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- December 29, 2023
Related products
- Ibuprofen And Famotidine – drug information
- NDC 67877-626 Ibuprofen and famotidine · Ibuprofen 800 mg/1; Famotidine 26.6 mg/1 · Ascend Laboratories, LLC