NDC 50228-126
Pramipexole Dihydrochloride 0.125 mg tablet
On the label: ScieGen Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Pramipexole: every company that makes it
- Form
- tablet, oral
- Strength
- 0.125 mg
- Approval
- ANDA ANDA203855
- On the market since
- Oct 29, 2014
- Package NDCs
50228-126-1050228-126-90- Official label
- DailyMed (National Library of Medicine), updated Dec 24, 2025
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