NDC 50090-3280
Pramipexole Dihydrochloride 0.25 mg tablet
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-181.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · relabels it
Product details
- Generic drug
- Pramipexole: every company that makes it
- Form
- tablet, oral
- Strength
- 0.25 mg
- Approval
- ANDA ANDA202633
- On the market since
- Oct 26, 2012
- Package NDCs
50090-3280-0- Official label
- DailyMed (National Library of Medicine), updated Sep 9, 2026
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