DIFTOSEC CT lyofilizát a rozpúšťadlo na injekčnú suspenziu pre kurčatá a morky
DIFTOSEC CT lyofilizát a rozpúšťadlo na injekčnú suspenziu pre kurčatá a morky
Authorised
- Fowlpox virus, strain DECP 25, Live
Product identification
Medicine name:
DIFTOSEC CT lyofilizát a rozpúšťadlo na injekčnú suspenziu pre kurčatá a morky
Active substance:
- Fowlpox virus, strain DECP 25, Live
Target species:
-
Chicken (broiler)
-
Chicken (pullet future breeder)
-
Chicken (pullet for egg production, future layer)
Route of administration:
-
Skin scarification
-
Transdermal use
Product details
Active substance and strength:
-
Fowlpox virus, strain DECP 25, Live3.00/log10 50% cell culture infectious dose0.01millilitre(s)
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Skin scarification
-
Chicken (broiler)
-
All relevant tissues0dayzero days
-
-
Chicken (pullet future breeder)
-
All relevant tissues0dayzero days
-
-
Chicken (pullet for egg production, future layer)
-
All relevant tissues0dayzero days
-
-
-
Transdermal use
-
Chicken (broiler)
-
All relevant tissues0dayzero days
-
-
Chicken (pullet future breeder)
-
All relevant tissues0dayzero days
-
-
Chicken (pullet for egg production, future layer)
-
All relevant tissues0dayzero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD12
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
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 Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/0019/98-S
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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Published on: 19/12/2023
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