Aurobindo Pharma Limited
Medchal, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.
NDC 50436-0147
Sumatriptan 50 mg tablet
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Aurobindo Pharma Limited's NDC 65862-147.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Sumatriptan: see every company that makes it
- Form
- tablet
- Strength
- 50 mg
- Approval
- ANDA ANDA078327
- On the market since
- Aug 17, 2009
- Package NDCs
50436-0147-1- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2018
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