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Silodosin Recordati (silodosin)

Generic
Region
🇪🇺 EU
Active substance
silodosin
Company
Recordati Ireland Ltd
Status
Authorised
Therapeutic area
Prostatic Hyperplasia
EU approval
Mon 07 Jan 2019
Designations
Generic
Application
EMEA/H/C/004964
ATC
G04CA04
Official record
www.ema.europa.eu

Indication

Treatment of the signs and symptoms of benign prostatic hyperplasia (BPH) in adult men.

Regulatory milestones

No milestones recorded in the last year.

Same substance in other markets

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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.