Home
>
National Drug Code (NDC)
>
Tekturna HCT
Tekturna HCT - 0078-0522-35 - (aliskiren hemifumarate and hydrochlorothiazide)
Drug Information of Tekturna HCT
| Product NDC: | 0078-0522 |
| Proprietary Name: | Tekturna HCT |
| Non Proprietary Name: | aliskiren hemifumarate and hydrochlorothiazide |
| Active Ingredient(s): | 150; 25 mg/1; mg/1 & nbsp; aliskiren hemifumarate and hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tekturna HCT
| Product NDC: | 0078-0522 |
| Labeler Name: | Novartis Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022107 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080801 |
Package Information of Tekturna HCT
| Package NDC: | 0078-0522-35 |
| Package Description: | 100 BLISTER PACK in 1 PACKAGE (0078-0522-35) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0522-61) |
NDC Information of Tekturna HCT
| NDC Code | 0078-0522-35 |
| Proprietary Name | Tekturna HCT |
| Package Description | 100 BLISTER PACK in 1 PACKAGE (0078-0522-35) > 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0522-61) |
| Product NDC | 0078-0522 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | aliskiren hemifumarate and hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080801 |
| Marketing Category Name | NDA |
| Labeler Name | Novartis Pharmaceuticals Corporation |
| Substance Name | ALISKIREN HEMIFUMARATE; HYDROCHLOROTHIAZIDE |
| Strength Number | 150; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Renin Inhibitor [EPC],Renin Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
