| NDC Code | 70710-1353-9 |
|---|
| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1353-9) |
|---|
| Product NDC | 70710-1353 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Tofacitinib |
|---|
| Non-Proprietary Name | Tofacitinib |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20250312 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA214264 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| Substance Name | TOFACITINIB CITRATE |
|---|
| Strength | 11 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Janus Kinase Inhibitor [EPC], Janus Kinase Inhibitors [MoA] |
|---|