| NDC Code | 71432-2002-1 |
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| Package Description | 1 BAG in 1 CARTON (71432-2002-1) / 5 BLISTER PACK in 1 BAG / 10 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK |
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| Product NDC | 71432-2002 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tacrolimus |
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| Non-Proprietary Name | Tacrolimus Extended-release Capsules |
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| Dosage Form | CAPSULE, COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20240125 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215012 |
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| Manufacturer | Chengdu Suncadia Medicine Co., Ltd. |
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| Substance Name | TACROLIMUS |
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| Strength | 1 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Calcineurin Inhibitor Immunosuppressant [EPC], Calcineurin Inhibitors [MoA] |
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