Tofacitinib 70069-0842
Product NDC
70069-0842- Manufacturer
- Somerset Therapeutics, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 3, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA220137
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tofacitinib Citrate | 10 mg/1 |
Drug Class
Janus Kinase Inhibitor [EPC]Janus Kinase Inhibitors [MoA]
Packaging Options(1)
60 TABLET, FILM COATED in 1 BOTTLE (70069-842-01)