Combimarv (insulin human)
- Region
- 🇪🇺 EU
- Active substance
- insulin human
- Company
- Marvel Life Sciences Ltd.
- Status
- Application withdrawn
- Application
- EMEA/H/C/002609
- Official record
- www.ema.europa.eu
Indication
Treatment of diabetes mellitus
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Insuman Authorised · Sanofi-aventis Deutschland GmbH
- 🇪🇺 Insulin Human Rechon Application withdrawn · Rechon Life Science AB
- 🇪🇺 Actraphane Authorised · Novo Nordisk A/S
- 🇪🇺 Mixtard Authorised · Novo Nordisk A/S
- 🇪🇺 Inpremzia Withdrawn · Baxter Holding B.V.
- 🇪🇺 Insulatard Authorised · Novo Nordisk A/S
- 🇪🇺 Protaphane Authorised · Novo Nordisk A/S
- 🇪🇺 Insulin Human Winthrop Withdrawn · sanofi-aventis Deutschland GmbH
- 🇪🇺 Solumarv Refused · Marvel Lifesciences Ltd
- 🇪🇺 Solumarv Application withdrawn · Marvel Life Sciences Ltd.
- 🇪🇺 Isomarv medium Application withdrawn · Marvel Life Sciences Ltd.
- 🇪🇺 Velosulin Withdrawn · Novo Nordisk A/S
Follow Combimarv
Get VigiEye Daily: approvals, opinions, safety actions and PDUFA dates every morning.
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.