NDC 16714-922
Pramipexole Dihydrochloride 4.5 mg tablet, extended release
On the label: Northstar Rx LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | District Solan, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action |
Product details
- Generic drug
- Pramipexole: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 4.5 mg
- Approval
- ANDA ANDA206156
- On the market since
- Mar 6, 2019
- Package NDCs
16714-922-01- Official label
- DailyMed (National Library of Medicine), updated Aug 20, 2024
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