VIMCO emulsion for injection for ewes and female goats
VIMCO emulsion for injection for ewes and female goats
Authorised
- Staphylococcus aureus, strain SP 140, Inactivated
Product identification
Medicine name:
VIMCO emulsion for injection for ewes and female goats
Vimco Emulsie voor injectie
Vimco Emulsion injectable
Vimco Emulsion zur Injektion
Active substance:
- Staphylococcus aureus, strain SP 140, Inactivated
Target species:
-
Sheep (ewe)
-
Goat (adult female)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Staphylococcus aureus, strain SP 140, Inactivated8.98/cells1.00Dose
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep (ewe)
-
Meat and offal0day
-
-
Goat (adult female)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI03AB
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- box containing 1 PET vial containing 50 doses (100 ml)
- box containing 1 PET vial containing 25 doses (50 ml)
- box containing 1 PET vial containing 5 doses (10 ml)
- box containing 1 glass vial containing 50 doses (100 ml)
- box containing 1 glass vial containing 25 doses (50 ml)
- box containing 1 glass vial containing 5 doses (10 ml)
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:
- Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- LABORATORIOS HIPRA, S.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0209/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Cyprus
-
France
-
Germany
-
Greece
-
Ireland
-
Italy
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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