Sun Pharmaceutical Industries, Inc. recalls Sumatriptan Succinate Tablets, 100 mg packaged in 9 (1X9) Unit-of-use blister card, (62756-0522-69), Rx only, Sun Pharm
Recalled January 22, 2020 · FDA recall D-0660-2020 · Sun Pharmaceutical Industries
Hazard
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance. · FDA Class II
Units
207,585 blisters
Sold at
Product was distributed throughout the United States to 96 distributors and 1 repacker/relabeler.
Description
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.
Product
Sumatriptan Succinate Tablets, 100 mg packaged in 9 (1X9) Unit-of-use blister card, (62756-0522-69), Rx only, Sun Pharma, Cranbury, NJ
Manufacturer(s)
Sun Pharmaceutical Industries, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →