NDC 33342-211
Pramipexole Dihydrochloride 2.25 mg tablet, extended release
On the label: Macleods Pharmaceuticals Limited.
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
- 2.25 mg
- Approval
- ANDA ANDA206156
- On the market since
- Aug 24, 2020
- Package NDCs
33342-211-0733342-211-12- Official label
- DailyMed (National Library of Medicine), updated Jul 6, 2024
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