| NDC Code | 13668-383-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (13668-383-05) |
|---|
| Product NDC | 13668-383 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide 40/10/12.5 Mg |
|---|
| Non-Proprietary Name | Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide Tablet 40/10/12.5 Mg |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20161026 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203580 |
|---|
| Manufacturer | Torrent Pharmaceuticals Limited |
|---|
| Substance Name | AMLODIPINE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL |
|---|
| Strength | 10; 12.5; 40 |
|---|
| Strength Unit | mg/1; 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], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|