Exondys 51

Active Ingredient(s): Eteplirsen
FDA Approved: * September 19, 2016
Category: Genetic Disorders

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

Exondys 51 Overview

Eteplirsen (brand name Exondys 51) is a medication to treat, but not cure, some types of Duchenne muscular dystrophy (DMD), caused by a specific mutation. Eteplirsen only targets specific mutations and can be used to treat about 14% of DMD cases.[1][2] Eteplirsen is a form of antisense therapy. Eteplirsen was developed by Sarepta Therapeutics. After a controversial debate surrounding the drug's efficacy, during which two FDA review panel members resigned in pro...

Read more Exondys 51 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/Eteplirsen

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Possible Dosages for this and Related Drugs:

  • Solution: 100mg/2ml (50mg/ml), 500mg/10ml (50mg/ml)
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Exondys 51: (2 results)

Sorted by National Drug Code
  • 60923-284 Exondys 51 50 mg/ml Intravenous Injection by Sarepta Therapeutics, Inc.
  • 60923-363 Exondys 51 50 mg/ml Intravenous Injection by Sarepta Therapeutics, Inc.

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

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