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  2. Viloxazine - Wikipedia

    en.wikipedia.org/wiki/Viloxazine

    [6] [1] [5] The immediate-release form has an elimination half-life of 2.5 hours [6] [2] while the half-life of the extended-release form is 7 hours. [1] Viloxazine was first described by 1972 [10] and was marketed as an antidepressant in Europe in 1974. [6] [11] It was not marketed in the United States at this time. [12]

  3. Sofosbuvir/velpatasvir - Wikipedia

    en.wikipedia.org/wiki/Sofosbuvir/velpatasvir

    Sofosbuvir/velpatasvir, sold under the brand name Epclusa among others, is a fixed-dose combination medication for the treatment of hepatitis C in adults. [2] [5] [6] [7] It combines sofosbuvir and velpatasvir. [2] [5] [6] It is more than 90% effective for hepatitis C genotypes one through six. [2]

  4. List of investigational attention deficit hyperactivity ...

    en.wikipedia.org/wiki/List_of_investigational...

    Pirepemat (IRL-752) – "cortical enhancer" / serotonin 5-HT 7 receptor antagonist and α 2C-adrenergic receptor antagonist, other actions [96] [97] Pozanicline (A-87089.0, ABT-089) – α 4 β 2 nicotinic acetylcholine receptor agonist [98] SEP-225432 – serotonin–norepinephrine–dopamine reuptake inhibitor [99]

  5. List of antidepressants - Wikipedia

    en.wikipedia.org/wiki/List_of_antidepressants

    This is a complete list of clinically approved prescription antidepressants throughout the world, as well as clinically approved prescription drugs used to augment antidepressants or mood stabilizers, by pharmacological and/or structural classification.

  6. US FDA approves Novo Nordisk's Ozempic to cut risk of ... - AOL

    www.aol.com/news/us-fda-approves-novo-nordisks...

    The U.S. Food and Drug Administration's approval makes the drug, chemically known as semaglutide, to become the first GLP-1 treatment option for people with type 2 diabetes and CKD.

  7. Drug Price Competition and Patent Term Restoration Act

    en.wikipedia.org/wiki/Drug_Price_Competition_and...

    Second, the Act allows the life of patents covering a drug to be extended by a portion of the time the drug is under regulatory review by the FDA, ensuring that regulatory review will not unduly consume patent life. [5] The Act also requires the drug innovator to give the FDA the numbers of patents it believes cover its drug; the FDA does not ...

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