| NDC Code | 76333-111-15 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (76333-111-15) |
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| Product NDC | 76333-111 |
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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 | 20260610 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA219830 |
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| Manufacturer | Orient Pharma Co., Ltd. Yunlin Plant |
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| Substance Name | TOFACITINIB CITRATE |
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| Strength | 11 |
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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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