NDC 50419-489
Nexavar 200 mg tablet, film coated
On the label: Bayer HealthCare Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bayer AG | Leverkusen, Germany | Makes it, tests it, packages it and mills it | Problems found, fixed voluntarilyMar 20, 2025 · 10 inspections, 2 with FDA action |
| Bayer AG | Wuppertal, Germany | Makes the active ingredient and tests it | Problems found, fixed voluntarilyJan 18, 2023 · 8 inspections |
| Patheon France S.A.S | Bourgoin Jallieu, France | Makes it | Problems found, fixed voluntarilySep 29, 2023 · 5 inspections |
| Sharp Packaging Services, LLC | Allentown, PA, United States | Packages it and labels it | No problems foundNov 21, 2025 · 7 inspections |
Product details
- Generic drug
- Sorafenib: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- NDA NDA021923
- On the market since
- Oct 2, 2023
- Package NDCs
50419-489-01- Official label
- DailyMed (National Library of Medicine), updated Aug 28, 2023
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