| NDC Code | 13668-251-74 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (13668-251-74) |
|---|
| Product NDC | 13668-251 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide 20/12.5 |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170424 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA206515 |
|---|
| Manufacturer | TORRENT PHARMACEUTICALS LIMITED |
|---|
| Substance Name | OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 20; 12.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
|---|