Levitra (vardenafil)
- Region
- 🇪🇺 EU
- Active substance
- vardenafil
- Company
- Bayer AG
- Status
- Authorised
- Therapeutic area
- Erectile Dysfunction
- EU approval
- Thu 06 Mar 2003
- Application
- EMEA/H/C/000475
- ATC
- G04BE09
- Official record
- www.ema.europa.eu
Indication
Treatment of erectile dysfunction in adult men. Erectile dysfunction is the inability to achieve or maintain a penile erection sufficient for satisfactory sexual performance. In order for Levitra to be effective, sexual stimulation is required. Levitra is not indicated for use by women.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Vivanza Withdrawn · Bayer AG
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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.