NDC 68462-331
Pramipexole dihydrochloride 0.25 mg tablet
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Pramipexole: every company that makes it
- Form
- tablet, oral
- Strength
- 0.25 mg
- Approval
- ANDA ANDA090781
- On the market since
- Oct 8, 2010
- Package NDCs
68462-331-0568462-331-1168462-331-90- Official label
- DailyMed (National Library of Medicine), updated Dec 30, 2025
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