Sun Pharmaceutical Industries, Inc. recalls Sumatriptan Succinate Tablets, 50 mg, packaged in a) 9 (1x9) Unit-of use blister card (NDC 62756-521-69) and b) 100 coun
Recalled January 22, 2020 · FDA recall D-0659-2020 · Sun Pharmaceutical Industries
Hazard
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance. · FDA Class II
Units
384/100 count bottles
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, 50 mg, packaged in a) 9 (1x9) Unit-of use blister card (NDC 62756-521-69) and b) 100 count bottles, (NDC 62756-521-88), 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 →