Zydus Lifesciences' Liquid Medicine For Treatment Of Severe Inherited Muscular Dystrophy Receives Final Approval From US Health Regulator
The approval by the US Food and Drug Administration (USFDA) is for Deflazacort oral suspension of strength 22.75 mg/ml, Zydus Lifesciences Ltd said in a regulatory filing.

File Image |
New Delhi: Zydus Lifesciences Ltd on Monday said it has received final approval from the US health regulator for its generic version of Deflazacort oral suspension used in treating a severe form of inherited muscular dystrophy.The approval by the US Food and Drug Administration (USFDA) is for Deflazacort oral suspension of strength 22.75 mg/ml, Zydus Lifesciences Ltd said in a regulatory filing.
Deflazacort oral suspension is indicated for treating Duchenne Muscular Dystrophy (DMD) in patients of five years of age and older.Deflazacort belongs to a group of medications called steroids. It works by decreasing inflammation and slowing down an overactive immune system.It will be produced at Doppel, Italy, the company said.
Disclaimer: This story is from the syndicated feed. Nothing has changed except the headline.
RECENT STORIES
-
Raksha Bandhan Special: Sister Donates Part Of Her Liver To Save Brother's Life In MP's Bhikangaon -
Lucknow Witnesses Grand Juloos-e-Mohammadi Processions On Eid Milad-un-Nabi -
Sayaji Hotel Indore Resumes Kitchen Operations After MP High Court Interim Order -
UP Govt To Lease Lucknow's JPNIC For 30 Years; Akhilesh Yadav Targets BJP -
UP Monsoon Impact: Lucknow Flooded, Gorakhpur Students Face Difficulties
