Vaxelis 0.5 ml, Injektionssuspension

7680669400033 CH-66940 Injektionssuspension
Vaxelis 0.5 ml, Injektionssuspension
Vaxelis 0.5 ml, Injektionssuspension
Vaxelis 0.5 ml, Injektionssuspension
1 / 3
google

Article details

Package size
10
Selling units
10
Measure
Fertigspritze(n)
Galenic form
Injektionssuspension
Galenic group
Injektion/Infusion

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Summary of Product Characteristics
Allemand
30/07/2026
Summary of Product Characteristics
Français
30/07/2026
Summary of Product Characteristics
Italien
30/07/2026

Detailed composition

Substance Quantity Type Category
polysaccharida haemophili influenzae typus B conjugata cum proteino neisseriae meningitidis B
53.0 UG Substance Wirkstoff (Principe actif)
polysaccharida haemophili influenzae typus B
3.0 UG Substance WIIS
neisseria meningitidis B outer membrane protein complex
50.0 UG Substance WIIS
hepatitidis B viri antigenum ADNr
10.0 UG Substance Wirkstoff (Principe actif)
toxoidum pertussis
20.0 UG Substance Wirkstoff (Principe actif)
haemagglutininum filamentosum
20.0 UG Substance Wirkstoff (Principe actif)
pertactinum
3.0 UG Substance Wirkstoff (Principe actif)
fimbriae
5.0 UG Substance Wirkstoff (Principe actif)
toxoidum diphtheriae
- Substance Wirkstoff (Principe actif)
toxoidum tetani
- Substance Wirkstoff (Principe actif)
virus poliomyelitis typus 1 inactivatus
29.0 U Substance Wirkstoff (Principe actif)
virus poliomyelitis typus 2 inactivatus
7.0 U Substance Wirkstoff (Principe actif)
virus poliomyelitis typus 3 inactivatus
26.0 U Substance Wirkstoff (Principe actif)
aluminium
- Substance HIMDK
aluminii phosphas
- Substance HNIDK
aluminii hydroxyphosphas sulfas amorphus
- Substance HNIDK
natrii phosphates
- Substance HNIDK
acidum hydrochloridum
- Substance HNIDK
natrii hydroxidum
- Substance HNIDK
aqua ad iniectabile
- Substance HNIDK
natrium
1.95 MG Substance HBESI
glutaralum
- Substance RESI
formaldehydum
- Substance RESI
neomycinum
- Substance RESI
streptomycinum
- Substance RESI
polymyxinum B
- Substance RESI
albuminum seri bovis
- Substance RESI
aluminii thiocyanas
- Substance RESI
faecis proteina
- Substance RESI

Authorization holder

Future Health Pharma GmbH

8620 Wetzikon ZH

Authorization information

Swissmedic authorization number
66940
Drug name
Vaxelis, Injektionssuspension
Galenic form
SUPA
ATC Code
J07CA09
Authorization status
Z
Dispensing category
B
First authorization
28/08/2019
Authorization expiration date
31/12/9999
IT Number
08.08.
Domain
Human medicine
Field of application
Grundimmunisierung und Auffrischimpfung bei Säuglingen und Kleinkindern ab einem Alter von 6 Wochen bis 4 Jahre (vor dem 5. Geburtstag) gegen Diphtherie, Tetanus, Pertussis, Hepatitis B, Poliomyelitis und durch Haemophilus influenzae Typ b (Hib) verursachte invasive Krankheiten.

Package details

Description (FR)
VAXELIS susp inj avec 1 aiguille 10 ser pré 0.5 ml
Description (DE)
VAXELIS Inj Susp mit 1 Nadel 10 Fertspr 0.5 ml
Market launch
28/08/2019
Narcotic (BTM)
No

Other package sizes (3)

VAXELIS susp inj av 2 aiguilles ser pré 0.5 ml
1 FESP
GTIN: 7680669400019
View
VAXELIS susp inj av 2 aiguilles 10 ser pré 0.5 ml
10 FESP
GTIN: 7680669400026
View
VAXELIS 0.5 ml susp inj 53 µg 1 pce
1 FESP
GTIN: 7680669400040
View
Buy us a coffee Explore the data