Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 with FDA action |
Product details
- Generic drug
- Sunitinib: every company that makes it
- Form
- capsule, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA215843
- On the market since
- Nov 30, 2022
- Package NDCs
43598-047-2843598-047-6343598-047-70- Official label
- DailyMed (National Library of Medicine), updated Mar 16, 2022
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