| NDC Code | 70839-325-30 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (70839-325-30) |
|---|
| Product NDC | 70839-325 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Tekturna Hct |
|---|
| Non-Proprietary Name | Aliskiren Hemifumarate And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20080801 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA022107 |
|---|
| Manufacturer | Noden Pharma USA, Inc. |
|---|
| Substance Name | ALISKIREN HEMIFUMARATE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 300; 25 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Increased Diuresis [PE], Renin Inhibitor [EPC], Renin Inhibitors [MoA], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|