NDC 68180-151
Mirabegron 25 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
- 25 mg
- Approval
- ANDA ANDA209485
- On the market since
- Apr 19, 2024
- Package NDCs
68180-151-0668180-151-09- Official label
- DailyMed (National Library of Medicine), updated Dec 24, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?