| NDC Code | 0378-1077-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (0378-1077-05) |
|---|
| Product NDC | 0378-1077 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Telmisartan And Amlodipine |
|---|
| Non-Proprietary Name | Telmisartan And Amlodipine |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140919 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202516 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | AMLODIPINE BESYLATE; TELMISARTAN |
|---|
| Strength | 5; 80 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
|---|