| NDC Code | 70710-1727-3 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1727-3) |
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| Product NDC | 70710-1727 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tofacitinib |
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| Non-Proprietary Name | Tofacitinib |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20250312 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA214264 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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| Substance Name | TOFACITINIB CITRATE |
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| Strength | 22 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Janus Kinase Inhibitor [EPC], Janus Kinase Inhibitors [MoA] |
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