Exondys 51

Active Ingredient(s): Eteplirsen
FDA Approved: * September 19, 2016
Pharm Company: * SAREPTA THERAPS INC
Category: Genetic Disorders

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 Steve Wilton, Sue Fletcher and colleagues at the University of Western Australia and commercialized by Sarepta Therapeutics.[3 ... [wikipedia]

* May have multiple approval dates, manufacturers, or labelers.
1 Discussion

Dosage List

Exondys 51 50 mg/ml Intravenous Injection
NDC: 60923-284
Labeler:
Sarepta Therapeutics, Inc.
Exondys 51 50 mg/ml Intravenous Injection
NDC: 60923-363
Labeler:
Sarepta Therapeutics, Inc.

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