Erysin Single Shot, emulzija za injekciju, za svinje
Erysin Single Shot, emulzija za injekciju, za svinje
Authorised
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated
- Erysipelothrix rhusiopathiae, serotype 1, strain 203, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated
Product identification
Medicine name:
Erysin Single Shot, emulzija za injekciju, za svinje
Active substance:
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated
- Erysipelothrix rhusiopathiae, serotype 1, strain 203, Inactivated
- Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated
Target species:
-
Pig
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-64, Inactivated1.00relative potency1.00Dose
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-5, Inactivated1.00relative potency1.00Dose
-
Erysipelothrix rhusiopathiae, serotype 1, strain 203, Inactivated1.00relative potency1.00Dose
-
Erysipelothrix rhusiopathiae, serotype 2, strain 2-II, Inactivated1.00relative potency1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Pig
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Croatia
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:
- Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
- UP/I-322-05/13-01/381
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Croatian (PDF)
Published on: 12/10/2023
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