NDC 68382-479
fesoterodine fumarate 4 mg tablet, film coated, extended release
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Fesoterodine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA204946
- On the market since
- Dec 7, 2017
- Package NDCs
68382-479-0668382-479-1668382-479-3068382-479-77- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2025
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