AD-LIVE-SUIVAX, κόνις και διαλύτης για ενέσιμο εναιώρημα
AD-LIVE-SUIVAX, κόνις και διαλύτης για ενέσιμο εναιώρημα
Authorised
- Aujeszky's disease virus, strain LomBart, Live
Product identification
Medicine name:
AD-LIVE-SUIVAX, κόνις και διαλύτης για ενέσιμο εναιώρημα
Active substance:
- Aujeszky's disease virus, strain LomBart, Live
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Aujeszky's disease virus, strain LomBart, Live5.50log10 tissue culture infective dose 502.00millilitre(s)
Pharmaceutical form:
-
Powder and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Pig
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 37646/05-11-1999/K-0126701
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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