| NDC Code | 70785-022-30 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (70785-022-30) |
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| Product NDC | 70785-022 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Duzallo |
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| Non-Proprietary Name | Lesinurad And Allopurinol |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20171003 |
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| End Marketing Date | 20191130 |
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| Marketing Category Name | NDA |
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| Application Number | NDA209203 |
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| Manufacturer | Ironwood Pharmaceuticals, Inc. |
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| Substance Name | LESINURAD; ALLOPURINOL |
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| Strength | 200; 300 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Urate Transporter 1 Inhibitor [EPC],Urate Transporter 1 Inhibitors [MoA],Cytochrome P450 3A Inducers [MoA],Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA] |
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