Uptravi

Active Ingredient(s): Selexipag
FDA Approved: * December 21, 2015
Pharm Company: * ACTELION PHARMS LTD
Category: Blood Pressure

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Uptravi Overview

Selexipag (brand name Uptravi) is a drug developed by Actelion for the treatment of pulmonary arterial hypertension (PAH). Selexipag and its active metabolite, ACT-333679 (or MRE-269, the free carboxylic acid), are agonists of the prostacyclin receptor, which leads to vasodilation in the pulmonary circulation.[1] ACT-333679 or MRE-269, the active metabolite of selexipag Contents 1 Contraindications 2 Adverse effects 3 History 4 See also 5 References Contraindicatio...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Selexipag

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Possible Dosages for this and Related Drugs:

NDC Database Records for Uptravi: (8 results)

Sorted by National Drug Code

• 66215-602 Uptravi 200 ug/1 Oral Tablet, Coated by Actelion Pharmaceuticals Us, Inc.
• 66215-604 Uptravi 400 ug/1 Oral Tablet, Coated by Actelion Pharmaceuticals Us, Inc.
• 66215-606 Uptravi 600 ug/1 Oral Tablet, Coated by Actelion Pharmaceuticals Us, Inc.
• 66215-608 Uptravi 800 ug/1 Oral Tablet, Coated by Actelion Pharmaceuticals Us, Inc.
• 66215-610 Uptravi 1000 ug/1 Oral Tablet, Coated by Actelion Pharmaceuticals Us, Inc.
• 66215-612 Uptravi 1200 ug/1 Oral Tablet, Coated by Actelion Pharmaceuticals Us, Inc.
• 66215-614 Uptravi 1400 ug/1 Oral Tablet, Coated by Actelion Pharmaceuticals Us, Inc.
• 66215-616 Uptravi 1600 ug/1 Oral Tablet, Coated by Actelion Pharmaceuticals Us, Inc.

Other drugs which contain Selexipag or a similar ingredient: (1 result)

• SELEXIPAG