Product identification
Medicine name:
Aftovaxpur DOE (25) A24 Cruzeiro + A Turkey 14/98
Active substance:
- Foot-and-mouth disease virus, serotype A, strain A24 Cruzeiro, Inactivated
- Foot-and-mouth disease virus, serotype A, strain Turkey 14/98, Inactivated
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Foot-and-mouth disease virus, serotype A, strain A24 Cruzeiro, InactivatedPresentation_strength:≥ 6 PD50 Reference:Hse Index:0
-
Foot-and-mouth disease virus, serotype A, strain Turkey 14/98, InactivatedPresentation_strength:≥ 6 PD50 Index:11
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Not applicable0dayZero days
-
- Sheep
-
Not applicable0dayZero days
-
- Pig
-
Not applicable0dayZero days
-
-
Subcutaneous use
- Cattle
-
Not applicable0dayZero days
-
- Sheep
-
Not applicable0dayZero days
-
- Pig
-
Not applicable0dayZero days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Package description:
- Packaging:Bottle (polypropylene), Package_size:10 bottles, Content:200 ml
- Packaging:Bottle (polypropylene), Package_size:1 bottle, Content:50 ml
- Packaging:Bottle (polypropylene), Package_size:1 bottle, Content:300 ml
- Packaging:Bottle (polypropylene), Package_size:1 bottle, Content:20 ml
- Packaging:Bottle (polypropylene), Package_size:10 bottles, Content:20 ml
- Packaging:Bottle (polypropylene), Package_size:1 bottle, Content:200 ml
- Packaging:Bottle (polypropylene), Package_size:10 bottles, Content:100 ml
- Packaging:Bottle (polypropylene), Package_size:10 bottles, Content:50 ml
- Packaging:Bottle (polypropylene), Package_size:10 bottles, Content:300 ml
- Packaging:Bottle (polypropylene), Package_size:1 bottle, Content:100 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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