Drug recall D-0534-2025
Product
Rizatriptan Benzoate Tablets, USP, 10 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd., INDIA, Distributed by: Ascend Laboratories LLC, Parsippany, NJ 07054, NDC 67877-262-18
Reason for recall
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
Lots and codes
Lot 22143653, 22143675, Exp Date: July 2025; Lot 22144528, Exp Date: September 2025; Lot 22144977, Exp Date: November 2025; Lot 23140257, Exp Date: December 2025; Lot 23140999, Exp Date: Feb. 2026; Lot 23141900, 23142118, 23142120, 23142123, Exp Date: May 2026; Lot 23144563, 23144565, Exp Date: November 2026; Lot 24142623, Exp Date: May 2027; Lot 24142624, 24142626, 24143469, Exp Date: Jun. 2027.
Recall details
- Recalling firm
- Ascend Laboratories, LLC, Bedminster, NJ
- Quantity
- N/A
- Distribution
- US Nationwide.
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 9, 2025
Related products
- Rizatriptan Benzoate – drug information
- NDC 67877-261 Rizatriptan Benzoate · Rizatriptan Benzoate 5 mg/1 · Ascend Laboratories, LLC
- NDC 67877-262 Rizatriptan Benzoate · Rizatriptan Benzoate 10 mg/1 · Ascend Laboratories, LLC