NDC 76333-111
Tofacitinib 11 mg tablet, film coated, extended release
On the label: Orient Pharma Co., Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Orient Pharma Co., Ltd. Yunlin Plant | Yunlin County, Taiwan | Makes it, tests it, packages it and labels it | No problems foundMay 23, 2025 · 4 inspections |
Product details
- Generic drug
- Tofacitinib: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 11 mg
- Approval
- ANDA ANDA219830
- On the market since
- Jun 10, 2026
- Package NDCs
76333-111-15- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2026
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