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 Description | UPTRAVI from Actelion Pharmaceuticals US, Inc. |
LABELER NAME: | Actelion Pharmaceuticals US, Inc. |
DEA SCHEDULE: |
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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: