FDA-Drug2020-01-22Class II
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
Sun Pharmaceutical Industries, Inc.
Hazard
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.
Sold states
Product was distributed throughout the United States to 96 distributors and 1 repacker/relabeler.
Affected count
384/100 count bottles
Manufactured in
270 Prospect Plains Rd, Cranbury, NJ, United States
Products
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
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0659-2020Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief