NDC 50090-2918
Selegiline Hydrochloride 5 mg tablet
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Apotex Corp.'s NDC 60505-3438.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apotex Inc. | Etobicoke, Canada | Makes it and tests it | No problems foundSep 27, 2024 · 9 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Product details
- Generic drug
- Selegiline: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA074871
- On the market since
- Jul 6, 1997
- Package NDCs
50090-2918-0- Official label
- DailyMed (National Library of Medicine), updated Feb 6, 2023
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