Suvaxyn MH-One Emulsion for injection for pigs
Suvaxyn MH-One Emulsion for injection for pigs
Not authorised
- Mycoplasma hyopneumoniae, strain P-5722-3, Inactivated
Product identification
Medicine name:
Suvaxyn MH-One Emulsion for injection for pigs
SUVAXYN MH-One, injekcinė emulsija kiaulėms
Active substance:
- Mycoplasma hyopneumoniae, strain P-5722-3, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Mycoplasma hyopneumoniae, strain P-5722-3, Inactivated1.00/relative unit(s)2.00millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI09AB13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Lithuania
Package description:
- (ID1): 1 Box with 1 Bottle (High Density PolyEthylene) with 20 millilitre(s) (20 millilitre(s))
- (ID6): 1 Box with 10 Bottle (High Density PolyEthylene) with 250 millilitre(s) (2500 millilitre(s))
- (ID2): 1 Box with 10 Bottle (High Density PolyEthylene) with 20 millilitre(s) (200 millilitre(s))
- (ID3): 1 Box with 1 Bottle (High Density PolyEthylene) with 100 millilitre(s) (100 millilitre(s))
- (ID4): 1 Box with 1 Bottle (High Density PolyEthylene) with 250 millilitre(s) (250 millilitre(s))
- (ID5): 1 Box with 10 Bottle (High Density PolyEthylene) with 100 millilitre(s) (1000 millilitre(s))
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/08/1822/001-003
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0248/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet