NDC 65862-767
Fesoterodine Fumarate 8 mg tablet, film coated, extended release
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Fesoterodine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 8 mg
- Approval
- ANDA ANDA205007
- On the market since
- Jun 17, 2022
- Package NDCs
65862-767-30- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?