CLASOVAX vaccino inattivato in sospensione iniettabile per bovini, ovini e caprini
CLASOVAX vaccino inattivato in sospensione iniettabile per bovini, ovini e caprini
Authorised
- Salmonella enterica, subsp. enterica, serovar Abortusovis, strain ATCC 31684, Inactivated
- Chlamydia abortus, strain AB7, Inactivated
- Chlamydia abortus, Inactivated
- Aluminium hydroxide
Product identification
Medicine name:
CLASOVAX vaccino inattivato in sospensione iniettabile per bovini, ovini e caprini
Active substance:
- Salmonella enterica, subsp. enterica, serovar Abortusovis, strain ATCC 31684, Inactivated
- Chlamydia abortus, strain AB7, Inactivated
- Chlamydia abortus, Inactivated
- Aluminium hydroxide
Target species:
-
Cattle
-
Goat
-
Sheep
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Salmonella enterica, subsp. enterica, serovar Abortusovis, strain ATCC 31684, Inactivated640.00/slow agglutination test unit(s)2.00millilitre(s)
-
Chlamydia abortus, strain AB7, Inactivated200.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Chlamydia abortus, Inactivated200.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
-
Aluminium hydroxide0.25/millilitre(s)2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
-
Subcutaneous use
-
Goat
-
Meat and offal0day
-
Milk0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI04AB
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
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:
- MSD Animal Health S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Syva S.A.
Responsible authority:
- Ministry Of Health
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
Combined File of all Documents
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Italian (PDF)
Published on: 24/07/2023