Active Ingredient(s): Solriamfetol
FDA Approved: * March 20, 2019
Category: Narcolepsy

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

Sunosi Overview

Solriamfetol, sold under the brand name Sunosi, is a medication used for the treatment of excessive sleepiness associated with narcolepsy and sleep apnea.[1] It is derived from d-phenylalanine and its chemical name is (R)-2-amino-3-phenylpropylcarbamate hydrochloride.[3] It is a norepinephrine–dopamine reuptake inhibitor (NDRI). Common side effects include headache, nausea, anxiety, and trouble sleeping.[1] The drug was discovered by a sub...

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Possible Dosages for this and Related Drugs:

  • Tablet: 150mg, 75mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Sunosi: (2 results)

Sorted by National Drug Code
  • 68727-350 Sunosi 75 mg Oral Tablet, Film Coated by Jazz Pharmaceuticals, Inc.
  • 68727-351 Sunosi 150 mg Oral Tablet, Film Coated by Jazz Pharmaceuticals, Inc.

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

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This information has been independently compiled and is for informational purposes only. It is not intended to be a substitute for medical advice from a qualified healthcare professional; nor is it intended to diagnose, treat, cure or prevent any disease. For more details please see the Medical Disclaimer. This page was last updated on 2 March 2021.

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