BODYGLOB injekčný roztok
BODYGLOB injekčný roztok
Authorised
- Immunoglobulins against Canine parvovirus, Canine
- Immunoglobulins against Canine distemper virus, Canine
- Immunoglobulins against Canine adenovirus 2, Canine
- Immunoglobulins against Canine parainfluenza virus, Canine
Product identification
Medicine name:
BODYGLOB injekčný roztok
Active substance:
- Immunoglobulins against Canine parvovirus, Canine
- Immunoglobulins against Canine distemper virus, Canine
- Immunoglobulins against Canine adenovirus 2, Canine
- Immunoglobulins against Canine parainfluenza virus, Canine
Target species:
-
Dog
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Immunoglobulins against Canine parvovirus, Canine512.00haemagglutination inhibiting unit(s)1.00millilitre(s)
-
Immunoglobulins against Canine distemper virus, Canine80.00log2 virus neutralising unit(s)1.00millilitre(s)
-
Immunoglobulins against Canine adenovirus 2, Canine64.00haemagglutination inhibiting unit(s)1.00millilitre(s)
-
Immunoglobulins against Canine parainfluenza virus, Canine32.00haemagglutination inhibiting unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Dog
-
-
Intravenous use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AM03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- Available only in Slovak
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:
- 97/044/04-S
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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Slovak (PDF)
Published on: 19/11/2021
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