Suivac APP2 injektionsvæske, emulsion
Suivac APP2 injektionsvæske, emulsion
Authorised
- Actinobacillus pleuropneumoniae, APX III toxoid
- Actinobacillus pleuropneumoniae, serotype 2, strain App2TR98, Inactivated
- Actinobacillus pleuropneumoniae, APX II toxoid
Product identification
Medicine name:
Suivac APP2 injektionsvæske, emulsion
Active substance:
- Actinobacillus pleuropneumoniae, APX III toxoid
- Actinobacillus pleuropneumoniae, serotype 2, strain App2TR98, Inactivated
- Actinobacillus pleuropneumoniae, APX II toxoid
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Actinobacillus pleuropneumoniae, APX III toxoid5.50enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Actinobacillus pleuropneumoniae, serotype 2, strain App2TR98, Inactivated5.50enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Actinobacillus pleuropneumoniae, APX II toxoid5.50enzyme-linked immunosorbent assay unit2.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
-
Meat and offal0day
-
Meat and offal0day
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Chemvet Dk A/S
Marketing authorisation date:
Manufacturing sites for batch release:
- Dyntec spol. s r.o.
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 66143
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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