ERYGAL P – injekčná emulzia
ERYGAL P – injekčná emulzia
Authorised
- Erysipelothrix rhusiopathiae, Inactivated
- Porcine parvovirus, Inactivated
Product identification
Medicine name:
ERYGAL P – injekčná emulzia
Active substance:
- Erysipelothrix rhusiopathiae, Inactivated
- Porcine parvovirus, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Erysipelothrix rhusiopathiae, Inactivated1.00/Protective Dose2.00millilitre(s)
-
Porcine parvovirus, Inactivated7.00/log2 haemagglutination inhibiting unit(s)2.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
All relevant tissues0dayzero days
-
-
-
Subcutaneous use
-
Pig
-
All relevant tissues0dayzero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AL03
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Pharmagal Bio spol. s r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Pharmagal Bio spol. s r.o.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 97/ 025/ 03-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: 13/12/2021