Anoro Ellipta (GlaxoSmithKline LLC)


Welcome to the PulseAid listing for the Anoro Ellipta drug offered from GlaxoSmithKline LLC. This 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: umeclidinium bromide and vilanterol trifenatate
SUBSTANCE NAME: UMECLIDINIUM BROMIDE; VILANTEROL TRIFENATATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: 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: 2014-01-31
END MARKETING DATE: 0000-00-00


Anoro Ellipta HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAnoro Ellipta from GlaxoSmithKline LLC
LABELER NAME: GlaxoSmithKline LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 62.5; 25(ug/1; ug/1)
START MARKETING DATE: 2014-01-31
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0173-0869_096cef06-00ef-4797-998b-20a93c6d0896
PRODUCT NDC: 0173-0869
APPLICATION NUMBER: NDA203975

Other UMECLIDINIUM BROMIDE; VILANTEROL TRIFENATATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GlaxoSmithKline LLCAnoro Ellipta