Triacelluvax (diphtheria, tetanus and pertussis (acellular, component) vaccine (adsorbed))
- Region
- 🇪🇺 EU
- Active substance
- diphtheria, tetanus and pertussis (acellular, component) vaccine (adsorbed)
- Company
- Chiron S.p.A.
- Status
- Withdrawn
- Therapeutic area
- Immunization; Tetanus; Whooping Cough; Diphtheria
- EU approval
- Mon 11 Jan 1999
- Application
- EMEA/H/C/000181
- ATC
- J07AJ
- Official record
- www.ema.europa.eu
Indication
TRIACELLUVAX is indicated for active immunisation of children from 6 weeks up to 7 years of age against diphtheria, tetanus and pertussis.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Infanrix Hexa Authorised · GlaxoSmithKline Biologicals S.A.
- 🇪🇺 Hexacima Authorised · Sanofi Winthrop Industrie
- 🇪🇺 Hexyon Authorised · Sanofi Winthrop Industrie
- 🇪🇺 Vaxelis Authorised · MCM Vaccine B.V.
- 🇪🇺 Tritanrix HepB Lapsed · GlaxoSmithKline Biologicals S.A.
- 🇪🇺 Infanrix Penta Lapsed · GlaxoSmithKline Biologicals S.A.
- 🇪🇺 Hexavac Withdrawn · Sanofi Pasteur MSD, SNC
- 🇪🇺 Quintanrix Withdrawn · GlaxoSmithKline Biologicals S.A.
- 🇪🇺 Infanrix HepB Withdrawn · GlaxoSmithKline Biologicals S.A.
- 🇪🇺 Primavax Withdrawn · Pasteur Mà¨rieux MSD
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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.