Zydus gets USFDA nod for Dutasteride Capsules

India Infoline News Service | Mumbai | October 07, 2017 10:07 IST

Zydus Cadila informed that it has received the final approval from the USFDA to market Dutasteride Capsules, 0.5 mg. It will be manufactured at the group’s formulations manufacturing facility at Moraiya, Ahmedabad.

Zydus Cadila informed that it has received the final approval from the USFDA to market Dutasteride Capsules, 0.5 mg. It will be manufactured at the group’s formulations manufacturing facility at Moraiya, Ahmedabad.
 
The drug is indicated for the treatment of sympotomatic benign prostatic hyperplasis (BPH) in men with an enlarged prostate to improve symptoms, reduce the risk of acute urinary retention (AUR) and reduce the risk of the need for BPH-related surgery.
 
The stock of Cadila Healthcare ended lower by 0.04% at Rs 500 per share on BSE on Friday. The stock touched its intraday high and low at Rs 504 and Rs 495.05 per share, respectively.
 
The group now has more than 160 approvals and has so far filed over 300 ANDAs since the commencement of the filing process in FY04.  

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