Trelegy Ellipta (GlaxoSmithKline LLC)


Welcome to the PulseAid listing for the Trelegy Ellipta drug offered from GlaxoSmithKline LLC. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [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: fluticasone furoate, umeclidinium bromide and vilanterol trifenatate
SUBSTANCE NAME: FLUTICASONE FUROATE; UMECLIDINIUM BROMIDE; VILANTEROL TRIFENATATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
ROUTE: RESPIRATORY (INHALATION)
DOSAGE FORM: POWDER
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2017-09-18
END MARKETING DATE: 0000-00-00


Trelegy Ellipta HUMAN PRESCRIPTION DRUG Details:

Item DescriptionTrelegy Ellipta from GlaxoSmithKline LLC
LABELER NAME: GlaxoSmithKline LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 100; 62.5; 25(ug/1; ug/1; ug/1)
START MARKETING DATE: 2017-09-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0173-0887_c550bb69-ea8e-4ff6-9b45-7c99e3eaad1b
PRODUCT NDC: 0173-0887
APPLICATION NUMBER: NDA209482

Other FLUTICASONE FUROATE; UMECLIDINIUM BROMIDE; VILANTEROL TRIFENATATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCTrelegy Ellipta