Tekturna (Novartis Pharmaceuticals Corporation)
Welcome to the PulseAid listing for the Tekturna drug offered from Novartis Pharmaceuticals Corporation. This Renin Inhibitor [EPC],Renin Inhibitors [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Novartis Pharmaceuticals Corporation |
| NON-PROPRIETARY NAME: | aliskiren hemifumarate |
| SUBSTANCE NAME: | ALISKIREN HEMIFUMARATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Renin Inhibitor [EPC],Renin Inhibitors [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | TABLET, FILM COATED |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2007-03-05 |
| END MARKETING DATE: | 0000-00-00 |
Tekturna HUMAN PRESCRIPTION DRUG Details:
| Item Description | Tekturna from Novartis Pharmaceuticals Corporation |
| LABELER NAME: | Novartis Pharmaceuticals Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 150(mg/1) |
| START MARKETING DATE: | 2007-03-05 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0078-0485_7728a56e-1ef0-48cd-bef7-ff51198e4e63 |
| PRODUCT NDC: | 0078-0485 |
| APPLICATION NUMBER: | NDA021985 |
Other ALISKIREN HEMIFUMARATE Pharmaceutical Manufacturers / Labelers:
