| NDC Code | 59922-631-01 |
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| Package Description | 200 TABLET, FILM COATED in 1 BOTTLE (59922-631-01) |
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| Product NDC | 59922-631 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Auryxia |
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| Non-Proprietary Name | Ferric Citrate |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20140917 |
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| Marketing Category Name | NDA |
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| Application Number | NDA205874 |
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| Manufacturer | Akebia Therapeutics, Inc. |
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| Substance Name | TETRAFERRIC TRICITRATE DECAHYDRATE |
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| Strength | 210 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA] |
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