| NDC Code | 68382-929-06 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (68382-929-06) |
|---|
| Product NDC | 68382-929 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amlodipine And Olmesartan Medoxomil |
|---|
| Non-Proprietary Name | Amlodipine And Olmesartan Medoxomil |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180104 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207771 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| Substance Name | AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL |
|---|
| Strength | 5; 40 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
|---|