SUTENT (Pfizer Laboratories Div Pfizer Inc)
Welcome to the PulseAid listing for the SUTENT drug offered from Pfizer Laboratories Div Pfizer Inc. This Kinase Inhibitor [EPC],Protein Kinase 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: | Pfizer Laboratories Div Pfizer Inc |
| NON-PROPRIETARY NAME: | Sunitinib malate |
| SUBSTANCE NAME: | SUNITINIB MALATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Kinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA] |
| ROUTE: | ORAL |
| DOSAGE FORM: | CAPSULE |
| MARKETING CATEGORY NAME: | NDA |
| START MARKETING DATE: | 2006-01-26 |
| END MARKETING DATE: | 0000-00-00 |
SUTENT HUMAN PRESCRIPTION DRUG Details:
| Item Description | SUTENT from Pfizer Laboratories Div Pfizer Inc |
| LABELER NAME: | Pfizer Laboratories Div Pfizer Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 12.5(mg/1) |
| START MARKETING DATE: | 2006-01-26 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0069-0550_fc8fc988-6d68-4f7b-b274-dd332905ad3d |
| PRODUCT NDC: | 0069-0550 |
| APPLICATION NUMBER: | NDA021938 |
Other SUNITINIB MALATE Pharmaceutical Manufacturers / Labelers:
