NDC 62332-004
Pramipexole Dihydrochloride 0.25 mg tablet
On the label: Alembic Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
Product details
- Generic drug
- Pramipexole: every company that makes it
- Form
- tablet, oral
- Strength
- 0.25 mg
- Approval
- ANDA ANDA078894
- On the market since
- Mar 22, 2016
- Package NDCs
62332-004-90- Official label
- DailyMed (National Library of Medicine), updated Nov 12, 2025
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