| NDC Code | 70839-312-30 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (70839-312-30) |
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| Product NDC | 70839-312 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tekturna Hct |
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| Non-Proprietary Name | Aliskiren Hemifumarate And Hydrochlorothiazide |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20080801 |
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| Marketing Category Name | NDA |
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| Application Number | NDA022107 |
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| Manufacturer | Noden Pharma USA, Inc. |
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| Substance Name | ALISKIREN HEMIFUMARATE; HYDROCHLOROTHIAZIDE |
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| Strength | 300; 12.5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Increased Diuresis [PE], Renin Inhibitor [EPC], Renin Inhibitors [MoA], Thiazide Diuretic [EPC], Thiazides [CS] |
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