NDC 0615-8552
Pramipexole dihydrochloride 0.5 mg tablet
On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-332.
Where the pills inside were 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 |
Repackaging site
- NCS HealthCare of KY, LLC dba Vangard Labs, Glasgow, KY, United States · repackages it
Product details
- Generic drug
- Pramipexole: every company that makes it
- Form
- tablet, oral
- Strength
- 0.5 mg
- Approval
- ANDA ANDA090781
- On the market since
- Oct 8, 2010
- Package NDCs
0615-8552-39- Official label
- DailyMed (National Library of Medicine), updated Oct 9, 2024
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