M+PAC
M+PAC
Authorised
- Mycoplasma hyopneumoniae, Inactivated
Product identification
Medicine name:
M+PAC
M+PAC
Active substance:
- Mycoplasma hyopneumoniae, Inactivated
Target species:
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Mycoplasma hyopneumoniae, Inactivated1.47/relative unit(s)1.00millilitre(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:
-
Valid
Authorised in:
-
Ireland
Package description:
- Box of 10 bottle of 200 ml
- Box of 5 bottle of 200 ml
- Box of 2 bottle of 200 ml
- Box of 1 bottle of 200 ml
- Box of 1 bottle of 50 ml
- Box of 10 bottle of 100 ml
- Box of 5 bottle of 100 ml
- Box of 2 bottle of 100 ml
- Box of 1 bottle of 100 ml
- Box of 10 bottles of 50 ml
- Box of 5 bottles of 50 ml
- Box of 2 bottles of 50 ml
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:
- Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Burgwedel Biotech GmbH
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10996/236/001
Date of authorisation status change:
Reference member state:
-
Hungary
Procedure number:
- HU/V/0140/001/MR
Concerned member states:
-
Austria
-
Belgium
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Germany
-
Greece
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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