Tofacitinib 70095-0008
Product NDC
70095-0008- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 3, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA218407
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tofacitinib Citrate | 1 mg/mL |
Drug Class
Janus Kinase Inhibitor [EPC]Janus Kinase Inhibitors [MoA]
Packaging Options(1)
1 BOTTLE in 1 CARTON (70095-008-02) / 240 mL in 1 BOTTLE