Aftovaxpur DOE (25) A24 Cruzeiro + A Turkey 14/98

Authorised

Foot-and-mouth disease virus, serotype A, strain A24 Cruzeiro, Inactivated
Foot-and-mouth disease virus, serotype A, strain Turkey 14/98, Inactivated

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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, Inactivated

Presentation_strength:≥ 6 PD50 Reference:Hse Index:0
Foot-and-mouth disease virus, serotype A, strain Turkey 14/98, Inactivated

Presentation_strength:≥ 6 PD50 Index:11

Pharmaceutical form:

Emulsion for injection

Withdrawal period by route of administration:

Intramuscular use
- Cattle
  - Not applicable
    
    0
    
    day
    
    Zero days
- Sheep
  - Not applicable
    
    0
    
    day
    
    Zero days
- Pig
  - Not applicable
    
    0
    
    day
    
    Zero days
Subcutaneous use
- Cattle
  - Not applicable
    
    0
    
    day
    
    Zero days
- Sheep
  - Not applicable
    
    0
    
    day
    
    Zero days
- Pig
  - Not applicable
    
    0
    
    day
    
    Zero days

Anatomical therapeutic chemical veterinary (ATCvet) codes:

QI02AA04

Legal status of supply:

Veterinary medicinal product subject to veterinary prescription

Authorisation status:

Valid

Authorised in:

Austria
Belgium
Bulgaria
Croatia
Cyprus
Czechia
Denmark
Estonia
Finland
France
Germany
Greece
Hungary
Iceland
Ireland
Italy
Latvia
Liechtenstein
Lithuania
Luxembourg
Malta
Netherlands
Norway
Poland
Portugal
Romania
Slovakia
Slovenia
Spain
Sweden
United Kingdom (Northern Ireland)

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)

Marketing authorisation holder:

Boehringer Ingelheim Vetmedica GmbH

Marketing authorisation issued:

15/07/2013

Manufacturing sites for batch release:

Boehringer Ingelheim Animal Health France

Authorisation country:

This information is not available for this product.

Responsible authority:

European Commission

Authorisation number:

This information is not available for this product.

Date of authorisation status change:

15/07/2013

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet