NDC 70518-4665
Mirabegron 50 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-152.
Where the pills inside were 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
- May 22, 2026
- Package NDCs
70518-4665-0- Official label
- DailyMed (National Library of Medicine), updated May 22, 2026
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