NDC 68180-152
Mirabegron 50 mg tablet, film coated, extended release
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Nagpur, India | Makes it and packages it | Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections |
Product details
- Generic drug
- Mirabegron: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA209485
- On the market since
- Sep 3, 2024
- Package NDCs
68180-152-0668180-152-09- Official label
- DailyMed (National Library of Medicine), updated Dec 24, 2025
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