Hetlioz Lq

Active Ingredient(s): Tasimelteon
FDA Approved: * December 1, 2020
Pharm Company: * VANDA PHARMS INC
Category: Sleep Aid

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

Hetlioz Lq Overview

Tasimelteon, sold under the brand name Hetlioz, is a medication approved by the U.S. Food and Drug Administration (FDA)[2] in January 2014, for the treatment of non-24-hour sleep–wake disorder (also called non-24, N24 and N24HSWD).[3] In June 2014, the European Medicines Agency (EMA) accepted an EU filing application for tasimelteon[4] and in July 2015, the drug was approved in the European Union for the treatment of non-24-hour sleep-wake...

Read more Hetlioz Lq Details
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/Tasimelteon

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Possible Dosages for this and Related Drugs:

  • Capsule: 20mg
  • Suspension: 4mg/ml
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Hetlioz Lq: (1 result)

Sorted by National Drug Code
  • 43068-304 Hetlioz 4 mg/ml Oral Suspension by Vanda Pharmaceuticals Inc.

Other drugs which contain Tasimelteon or a similar ingredient: (2 results)

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