Neofordex (dexamethasone)
- Region
- 🇪🇺 EU
- Active substance
- dexamethasone
- Company
- THERAVIA
- Status
- Authorised
- Therapeutic area
- Multiple Myeloma
- CHMP opinion
- Thu 17 Dec 2015
- EU approval
- Wed 16 Mar 2016
- Application
- EMEA/H/C/004071
- ATC
- H02AB02
- Official record
- www.ema.europa.eu
Indication
Treatment of multiple myeloma.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Ozurdex Authorised · AbbVie Deutschland GmbH & Co. KG
- 🇪🇺 Dexamethasone Taw Application withdrawn · Taw Pharma (Ireland) Ltd
- 🇪🇺 Neofordex Application withdrawn · Laboratoires CTRS - Boulogne Billancourt
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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.