| NDC Code | 0078-0605-35 |
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| Package Description | 100 BLISTER PACK in 1 PACKAGE (0078-0605-35) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0605-61) |
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| Product NDC | 0078-0605 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Tekamlo |
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| Non-Proprietary Name | Aliskiren Hemifumarate And Amlodipine Besylate |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20100101 |
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| End Marketing Date | 20150930 |
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| Marketing Category Name | NDA |
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| Application Number | NDA022545 |
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| Manufacturer | Novartis Pharmaceuticals Corporation |
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| Substance Name | ALISKIREN HEMIFUMARATE; AMLODIPINE BESYLATE |
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| Strength | 300; 5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Renin Inhibitor [EPC],Renin Inhibitors [MoA],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
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