UTIBRON NEOHALER (Novartis Pharmaceuticals Corporation)


Welcome to the PulseAid listing for the UTIBRON NEOHALER drug offered from Novartis Pharmaceuticals Corporation. This Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC],Anticholinergic [EPC],Cholinergic 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: Novartis Pharmaceuticals Corporation
NON-PROPRIETARY NAME: indacaterol and glycopyrrolate
SUBSTANCE NAME: INDACATEROL MALEATE; GLYCOPYRROLATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA]
ROUTE: RESPIRATORY (INHALATION)
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2015-10-29
END MARKETING DATE: 0000-00-00


UTIBRON NEOHALER HUMAN PRESCRIPTION DRUG Details:

Item DescriptionUTIBRON NEOHALER from Novartis Pharmaceuticals Corporation
LABELER NAME: Novartis Pharmaceuticals Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 27.5; 15.6(ug/1; ug/1)
START MARKETING DATE: 2015-10-29
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0078-0664_4407913f-f885-4308-a863-5e9b5365ea66
PRODUCT NDC: 0078-0664
APPLICATION NUMBER: NDA207930

Other INDACATEROL MALEATE; GLYCOPYRROLATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Novartis Pharmaceuticals CorporationUTIBRON NEOHALER