Ultratard (insulin human (rDNA))
- Region
- 🇪🇺 EU
- Active substance
- insulin human (rDNA)
- Company
- Novo Nordisk A/S
- Status
- Withdrawn
- Therapeutic area
- Diabetes Mellitus
- EU approval
- Mon 07 Oct 2002
- Application
- EMEA/H/C/000439
- ATC
- A10AE01
- 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
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- 🇪🇺 Mixtard Authorised · Novo Nordisk A/S
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- 🇪🇺 Insulatard Authorised · Novo Nordisk A/S
- 🇪🇺 Protaphane Authorised · Novo Nordisk A/S
- 🇪🇺 Velosulin Withdrawn · Novo Nordisk A/S
- 🇪🇺 Monotard Withdrawn · Novo Nordisk A/S
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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.