NDC 62756-520
sumatriptan succinate 25 mg tablet, film coated
On the label: Sun Pharmaceutical Industries, Inc..
FDA lists this product, but its label isn't on DailyMed yet, so we can't show its factories. They usually appear within a few weeks.
Where it's made
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer. - Dec 26, 2019 · Class II · Sun Pharmaceutical Industries, Inc.
Failed Impurities/Degradation Specifications; out-of-specification results obtained for related substance.
Lots: a) JKU1939A, JKU1940A, JKU1940B, exp. date 04/2022 and b) JKT4175A, exp. date 11/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sumatriptan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA078295
- On the market since
- Aug 10, 2009
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?