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Boostrix Polio, Injektionssuspension - 10
00681004 GlaxoSmithKline AG
Boostrix Polio, Injektionssuspension01.04.2004
  01.04.2004
Diphtheria-Pertussis-Poliomyelitis-Tetanus (J07CA02) 
WHO-DDD 
08.08.10
08.08. 
B  
No 
IP 
PR  
k.A.PR
  
7680006810044Impfstoffe
  
Composition
toxoidum diphtheriae ≥ 2 U.I., toxoidum tetani ≥ 20 U.I., toxoidum pertussis 8 µg, haemagglutininum filamentosum von Bordetella pertussis 8 µg, pertactinum von Bordetella pertussis 2.5 µg, virus poliomyelitis typus 1 inactivatus 40 U., virus poliomyelitis typus 2 inactivatus 8 U., virus poliomyelitis typus 3 inactivatus 32 U., natrii chloridum corresp. natrium 1.8 mg, aluminium 0.5 mg ut aluminii hydroxidum hydricum ad adsorptionem et aluminii phosphas, medium 199, aqua ad iniectabile q.s. ad suspensionem pro 0.5 ml, residui: neomycini sulfas, polymyxini B sulfas, polysorbatum 80, formaldehydum.
Packungsbestandteile
Active Agent
Vaccinum Diphtheriae Adsorbatum
Vaccinum Pertussis Acell. Adsorbatum
Vaccinum Poliomyelitidis Inactivatum (Salk typ I, II, III)
Vaccinum Tetani Adsorbatum
BAG: Active Agent
Vaccinum Diphtheriae Adsorbatum
Vaccinum Pertussis Acell. Adsorbatum
Vaccinum Poliomyelitidis Inactivatum (Salk typ I, II, III)
Vaccinum Tetani Adsorbatum
Source
Data was imported : 05.01.2024 Swissmedic Registration : Sequence : Product name : Registration owner: : Product group : Index Therapeuticus (BSV) : Medication Code : Date of registration : Valid until : Package number : Show package size : Commercial Form/Unit : Swissmedic categorie. : Active Agents : Composition :
 
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