Exondys 51
Active Ingredient(s): EteplirsenFDA 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 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 efficacy, during which two FDA review panel members resigned in protest, e...
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
Recent Exondys 51 Forums:
Be the first to start a discussion about this drug.Possible Dosages for this and Related Drugs:
Eteplirsen
- Solution: 100mg/2ml (50mg/ml), 500mg/10ml (50mg/ml)
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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512 Watson 353
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51 37 scored round white pill with v on other side
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