FDA Drug recall 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 627…
- FDA Drug
- Class II
- terminated
- Published 2020-01-22
On 2020-01-22 the FDA classified a Class II recall of 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 627… by Sun Pharmaceutical Industries, citing failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0659-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-26 |
| Published | 2020-01-22 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Sun Pharmaceutical Industries |
| Distribution | US |
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
Reason
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.
Identifiers
| ndc | 62756-520-83 |
|---|---|
| ndc | 62756-520-88 |
| ndc | 62756-520-08 |
| ndc | 62756-520-18 |
| ndc | 62756-520-69 |
| ndc | 62756-520-93 |
| ndc | 62756-520-01 |
| ndc | 62756-521-83 |
| ndc | 62756-521-88 |
| ndc | 62756-521-08 |
| ndc | 62756-521-18 |
| ndc | 62756-521-69 |
| ndc | 62756-521-93 |
| ndc | 62756-521-01 |
| ndc | 62756-522-83 |
| ndc | 62756-522-88 |
| ndc | 62756-522-08 |
| ndc | 62756-522-18 |
| ndc | 62756-522-69 |
| ndc | 62756-522-93 |
| ndc | 62756-522-01 |
| code_info | a) JKU1939A, JKU1940A, JKU1940B, exp. date 04/2022 and b) JKT4175A, exp. date 11/2020 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0659-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.