NDC 76420-093
Sumatriptan Succinate 50 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-292.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · relabels it
Product details
- Generic drug
- Sumatriptan: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA076847
- On the market since
- Nov 17, 2009
- Package NDCs
76420-093-09- Official label
- DailyMed (National Library of Medicine), updated Oct 24, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?