UPTRAVI (Actelion Pharmaceuticals US, Inc.)


Welcome to the PulseAid listing for the UPTRAVI drug offered from Actelion Pharmaceuticals US, Inc.. This Prostacyclin Receptor Agonist [EPC],Prostacyclin Receptor Agonists [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: Actelion Pharmaceuticals US, Inc.
NON-PROPRIETARY NAME: Selexipag
SUBSTANCE NAME: SELEXIPAG
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Prostacyclin Receptor Agonist [EPC],Prostacyclin Receptor Agonists [MoA]
ROUTE: ORAL
DOSAGE FORM: TABLET, COATED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2015-12-21
END MARKETING DATE: 0000-00-00


UPTRAVI HUMAN PRESCRIPTION DRUG Details:

Item DescriptionUPTRAVI from Actelion Pharmaceuticals US, Inc.
LABELER NAME: Actelion Pharmaceuticals US, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 200(ug/1)
START MARKETING DATE: 2015-12-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 66215-602_74fb8ee2-0162-4b76-b542-1dacf580fb63
PRODUCT NDC: 66215-602
APPLICATION NUMBER: NDA207947

Other SELEXIPAG Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Actelion Pharmaceuticals US, Inc.UPTRAVI