NDC 70710-1727
tofacitinib 22 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 voluntarilyMar 24, 2023 · 5 inspections |
Product details
- Generic drug
- Tofacitinib: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 22 mg
- Approval
- ANDA ANDA214264
- On the market since
- May 20, 2026
- Package NDCs
70710-1727-370710-1727-9- Official label
- DailyMed (National Library of Medicine), updated Oct 9, 2026
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