| NDC Code | 0378-1721-77 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1721-77) |
|---|
| Product NDC | 0378-1721 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amlodipine Besylate And Valsartan |
|---|
| Non-Proprietary Name | Amlodipine Besylate And Valsartan |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150330 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090483 |
|---|
| Manufacturer | Mylan Pharmaceuticals Inc. |
|---|
| Substance Name | AMLODIPINE BESYLATE; VALSARTAN |
|---|
| Strength | 5; 160 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
|---|