ARRANON (GlaxoSmithKline LLC)


Welcome to the PulseAid listing for the ARRANON drug offered from GlaxoSmithKline LLC. 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: GlaxoSmithKline LLC
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: 2006-01-19
END MARKETING DATE: 2018-12-31


ARRANON HUMAN PRESCRIPTION DRUG Details:

Item DescriptionARRANON from GlaxoSmithKline LLC
LABELER NAME: GlaxoSmithKline LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 5(mg/mL)
START MARKETING DATE: 2006-01-19
END MARKETING DATE: 2018-12-31
PRODUCT ID: 0007-4401_22b8c921-10d4-4a4f-9811-384d2b98853b
PRODUCT NDC: 0007-4401
APPLICATION NUMBER: NDA021877

Other NELARABINE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCARRANON
Novartis Pharmaceuticals CorporationArranon