NDC 50090-2497
Sumatriptan 6 mg per 0.5 mL injection
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0143-9638.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Farmaceutica (portugal), S.a | Terrugem Sintra, Portugal | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 21, 2023 · 9 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Product details
- Generic drug
- Sumatriptan: every company that makes it
- Form
- injection, subcutaneous
- Strength
- 6 mg per 0.5 mL
- Approval
- ANDA ANDA200183
- On the market since
- Sep 16, 2013
- Package NDCs
50090-2497-0- Official label
- DailyMed (National Library of Medicine), updated Jan 7, 2024
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