Emadine (emedastine)
- Region
- 🇪🇺 EU
- Active substance
- emedastine
- Company
- Immedica Pharma AB
- Status
- Authorised
- Therapeutic area
- Conjunctivitis, Allergic
- EU approval
- Wed 27 Jan 1999
- Application
- EMEA/H/C/000223
- ATC
- S01GX06
- Official record
- www.ema.europa.eu
Indication
Symptomatic treatment of seasonal allergic conjunctivitis.
Regulatory milestones
No milestones recorded in the last year.
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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.