Heptavac P Plus
Heptavac P Plus
Authorised
- Bibersteinia trehalosi, Inactivated
- Mannheimia haemolytica, serotype A1, Inactivated
- Clostridium chauvoei, strain 655, cells and equivalent toxoid
- Clostridium novyi, toxoid
- Clostridium tetani, toxoid
- Clostridium septicum, toxoid
- Clostridium perfringens, epsilon toxoid
- Clostridium perfringens, beta toxoid
- Mannheimia haemolytica, serotype A7, Inactivated
- Mannheimia haemolytica, serotype A9, Inactivated
- Mannheimia haemolytica, serotype A6, Inactivated
- Mannheimia haemolytica, serotype A2, Inactivated
Product identification
Medicine name:
Heptavac P Plus
Heptavac P
Active substance:
- Bibersteinia trehalosi, Inactivated
- Mannheimia haemolytica, serotype A1, Inactivated
- Clostridium chauvoei, strain 655, cells and equivalent toxoid
- Clostridium novyi, toxoid
- Clostridium tetani, toxoid
- Clostridium septicum, toxoid
- Clostridium perfringens, epsilon toxoid
- Clostridium perfringens, beta toxoid
- Mannheimia haemolytica, serotype A7, Inactivated
- Mannheimia haemolytica, serotype A9, Inactivated
- Mannheimia haemolytica, serotype A6, Inactivated
- Mannheimia haemolytica, serotype A2, Inactivated
Target species:
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Bibersteinia trehalosi, Inactivated500000000.00/cells1.00millilitre(s)
-
Mannheimia haemolytica, serotype A1, Inactivated500000000.00/cells1.00millilitre(s)
-
Clostridium chauvoei, strain 655, cells and equivalent toxoid0.50/Protective Dose1.00millilitre(s)
-
Clostridium novyi, toxoid3.50/international unit(s)1.00millilitre(s)
-
Clostridium tetani, toxoid2.50/international unit(s)1.00millilitre(s)
-
Clostridium septicum, toxoid2.50/international unit(s)1.00millilitre(s)
-
Clostridium perfringens, epsilon toxoid5.00/international unit(s)1.00millilitre(s)
-
Clostridium perfringens, beta toxoid1.00/international unit(s)1.00millilitre(s)
-
Mannheimia haemolytica, serotype A7, Inactivated50000.00/cells1.00millilitre(s)
-
Mannheimia haemolytica, serotype A9, Inactivated50000.00/cells1.00millilitre(s)
-
Mannheimia haemolytica, serotype A6, Inactivated50000.00/cells1.00millilitre(s)
-
Mannheimia haemolytica, serotype A2, Inactivated50000.00/cells1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI04AB05
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Package description:
- Low density polyethylene bottle of 500 ml with rubber closure and aluminium cap.
- Low density polyethylene bottle of 250 ml with rubber closure and aluminium cap.
- Low density polyethylene bottle of 100 ml with rubber closure and aluminium cap.
- Low density polyethylene bottle of 50 ml with rubber closure and aluminium cap.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- MSD Animal Health S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Ministry Of Health
Authorisation number:
- 102438
Date of authorisation status change:
Reference member state:
-
Italy
Procedure number:
- IT/V/0136/001
Concerned member states:
-
Greece
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 10/04/2024
Italian (PDF)
Published on: 10/04/2024