NDC 71205-251
sumatriptan succinate 50 mg tablet, film coated
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Sun Pharmaceutical Industries, Inc.'s NDC 62756-521.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sun Pharmaceutical Industries, Inc. names for other drugs.
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
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
- 50 mg
- Approval
- ANDA ANDA078295
- On the market since
- Aug 10, 2009
- Package NDCs
71205-251-09- Official label
- DailyMed (National Library of Medicine), updated Mar 1, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?