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 DescriptionArranon from Novartis Pharmaceuticals Corporation
LABELER NAME: Novartis Pharmaceuticals Corporation
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCARRANON
Novartis Pharmaceuticals CorporationArranon