| NDC Code | 0078-0606-34 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (0078-0606-34) |
|---|
| Product NDC | 0078-0606 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Tekamlo |
|---|
| Non-Proprietary Name | Aliskiren Hemifumarate And Amlodipine Besylate |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100101 |
|---|
| End Marketing Date | 20151031 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA022545 |
|---|
| Manufacturer | Novartis Pharmaceuticals Corporation |
|---|
| Substance Name | ALISKIREN HEMIFUMARATE; AMLODIPINE BESYLATE |
|---|
| Strength | 300; 10 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Renin Inhibitor [EPC],Renin Inhibitors [MoA],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
|---|