FDAFDA · Food and drugs·Recall number D-0659-2020
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
Published January 22, 2020 · Recall initiated: December 26, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SUMATRIPTAN SUCCINATE
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Distributor
- Product was distributed throughout the United States to 96 distributors and 1 repacker/relabeler.
- UPC
- 0362756521889
- Lot
- a) JKU1939A, JKU1940A, JKU1940B, exp. date 04/2022 and b) JKT4175A, exp. date 11/2020
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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