Exondys 51

Active Ingredient(s): Eteplirsen
FDA Approved: * September 19, 2016
Pharm Company: * SAREPTA THERAPS INC
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 a cure, some types of Duchenne muscular dystrophy (DMD), caused by a specific mutation. Eteplirsen only targets specific mutations and thus is only useful in just over 1% of cases.[1] After a debate surrounding the efficacy of the drug, eteplirsen received accelerated approval from the US Food and Drug administration in late 2016.[2][3] A year's worth of treatment is expected t...

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:

Eteplirsen
  • 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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