Arranon (Novartis Pharmaceuticals Corporation)
Welcome to the PulseAid listing for the Arranon drug offered from Novartis Pharmaceuticals Corporation. This Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] 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: | nelarabine |
SUBSTANCE NAME: | NELARABINE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
ROUTE: | INTRAVENOUS |
DOSAGE FORM: | INJECTION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2016-10-05 |
END MARKETING DATE: | 0000-00-00 |
Arranon HUMAN PRESCRIPTION DRUG Details:
Item Description | Arranon from Novartis Pharmaceuticals Corporation |
LABELER NAME: | Novartis Pharmaceuticals Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 5(mg/mL) |
START MARKETING DATE: | 2016-10-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0078-0683_aa41d999-2473-40e9-842e-c8b98ecb27c2 |
PRODUCT NDC: | 0078-0683 |
APPLICATION NUMBER: | NDA021877 |
Other NELARABINE Pharmaceutical Manufacturers / Labelers: