NDC 60429-086
Pramipexole Dihydrochloride 0.25 mg tablet
On the label: Golden State Medical Supply, Inc.. It's repackaged: Golden State Medical Supply, Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-127.
Where the pills inside were 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 |
Repackaging site
- Golden State Medical Supply Inc., Camarillo, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Pramipexole: every company that makes it
- Form
- tablet, oral
- Strength
- 0.25 mg
- Approval
- ANDA ANDA203855
- On the market since
- Oct 28, 2014
- Package NDCs
60429-086-90- Official label
- DailyMed (National Library of Medicine), updated Jan 26, 2026
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