Uptravi
Active Ingredient(s): SelexipagFDA 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] Contents 1 Contraindications 2 Adverse effects 3 History 4 Society and culture 4.1 Economics 5 See also 6 References 7 External links Contraindications In E...
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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Selexipag
- Tablet: 0.2mg, 0.4mg, 0.6mg, 0.8mg, 1.2mg, 1.4mg, 1.6mg, 1000mcg, 1200mcg, 1400mcg, 1600mcg, 1mg, 200mcg, 400mcg, 600mcg, 800mcg
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.