Yentreve (duloxetine)
- Region
- 🇪🇺 EU
- Active substance
- duloxetine
- Company
- Eli Lilly Nederland B.V.
- Status
- Authorised
- Therapeutic area
- Urinary Incontinence, Stress
- EU approval
- Wed 11 Aug 2004
- Application
- EMEA/H/C/000545
- ATC
- N06AX21
- Official record
- www.ema.europa.eu
Indication
Yentreve is indicated for women for the treatment of moderate to severe stress urinary incontinence (SUI).
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Duloxetine Viatris (previously Duloxetine Mylan) Authorised · Viatris Limited
- 🇺🇸 Duloxetine Hydrochloride Approved · Almatica
- 🇪🇺 Duloxetine Zentiva Authorised · Zentiva k.s.
- 🇪🇺 Duloxetine Lilly Authorised · Eli Lilly Nederland B.V.
- 🇪🇺 Cymbalta Authorised · Eli Lilly Nederland B.V.
- 🇪🇺 Nodetrip (previously Xeristar) Withdrawn · Esteve Pharmaceuticals, S.A.
- 🇪🇺 Ariclaim Withdrawn · Eli Lilly Nederland B.V.
- 🇪🇺 Duloxetine Sandoz Application withdrawn · Sandoz GmbH
- 🇪🇺 Duloxetine Boehringer Ingelheim Withdrawn · Boehringer Ingelheim International GmbH
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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.