Nucala (GlaxoSmithKline LLC)


Welcome to the PulseAid listing for the Nucala drug offered from GlaxoSmithKline LLC. This Interleukin-5 Antagonist [EPC],Interleukin-5 Antagonists [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: GlaxoSmithKline LLC
NON-PROPRIETARY NAME: mepolizumab
SUBSTANCE NAME: MEPOLIZUMAB
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Interleukin-5 Antagonist [EPC],Interleukin-5 Antagonists [MoA]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, POWDER, FOR SOLUTION
MARKETING CATEGORY NAME: BLA
START MARKETING DATE: 2015-11-04
END MARKETING DATE: 0000-00-00


Nucala HUMAN PRESCRIPTION DRUG Details:

Item DescriptionNucala from GlaxoSmithKline LLC
LABELER NAME: GlaxoSmithKline LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 100(mg/mL)
START MARKETING DATE: 2015-11-04
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0173-0881_3663c3fb-5ee9-429c-be9b-4767601a7c8f
PRODUCT NDC: 0173-0881
APPLICATION NUMBER: BLA125526

Other MEPOLIZUMAB Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCNucala