Heptavac P plus Injektionssuspension für Schafe
Heptavac P plus Injektionssuspension für Schafe
Authorised
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium septicum, toxoid
- Tetanus toxoid adsorbed
- Clostridium novyi, toxoid
- Clostridium chauvoei, cells and toxin, Inactivated
- Mannheimia haemolytica, serotype A1, strain S1006/77, Inactivated
- Mannheimia haemolytica, serotype A2, strain S1126/92, Inactivated
- Mannheimia haemolytica, serotype A6, strain S1084/81, Inactivated
- Mannheimia haemolytica, serotype A7, strain S1078/81, Inactivated
- Mannheimia haemolytica, serotype A9, strain S994/77, Inactivated
- Bibersteinia trehalosi, serotype T4, strain S1085/81, Inactivated
- Bibersteinia trehalosi, serotype T3, strain S1109/84, Inactivated
- Bibersteinia trehalosi, serotype T10, strain S1075/81, Inactivated
- Bibersteinia trehalosi, serotype T15, strain S1105/84, Inactivated
Product identification
Medicine name:
Heptavac P plus Injektionssuspension für Schafe
Active substance:
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium septicum, toxoid
- Tetanus toxoid adsorbed
- Clostridium novyi, toxoid
- Clostridium chauvoei, cells and toxin, Inactivated
- Mannheimia haemolytica, serotype A1, strain S1006/77, Inactivated
- Mannheimia haemolytica, serotype A2, strain S1126/92, Inactivated
- Mannheimia haemolytica, serotype A6, strain S1084/81, Inactivated
- Mannheimia haemolytica, serotype A7, strain S1078/81, Inactivated
- Mannheimia haemolytica, serotype A9, strain S994/77, Inactivated
- Bibersteinia trehalosi, serotype T4, strain S1085/81, Inactivated
- Bibersteinia trehalosi, serotype T3, strain S1109/84, Inactivated
- Bibersteinia trehalosi, serotype T10, strain S1075/81, Inactivated
- Bibersteinia trehalosi, serotype T15, strain S1105/84, Inactivated
Target species:
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clostridium perfringens, type C, beta toxoid10.00/international unit(s)1.00millilitre(s)
-
Clostridium perfringens, type D, epsilon toxoid5.00/international unit(s)1.00millilitre(s)
-
Clostridium septicum, toxoid2.50/international unit(s)1.00millilitre(s)
-
Tetanus toxoid adsorbed2.50/international unit(s)1.00millilitre(s)
-
Clostridium novyi, toxoid3.50/international unit(s)1.00millilitre(s)
-
Clostridium chauvoei, cells and toxin, Inactivated0.50/90% protective dose in guinea pig1.00millilitre(s)
-
Mannheimia haemolytica, serotype A1, strain S1006/77, Inactivated500000000.00/cells1.00millilitre(s)
-
Mannheimia haemolytica, serotype A2, strain S1126/92, Inactivated500000000.00/cells1.00millilitre(s)
-
Mannheimia haemolytica, serotype A6, strain S1084/81, Inactivated500000000.00/cells1.00millilitre(s)
-
Mannheimia haemolytica, serotype A7, strain S1078/81, Inactivated500000000.00/cells1.00millilitre(s)
-
Mannheimia haemolytica, serotype A9, strain S994/77, Inactivated500000000.00/cells1.00millilitre(s)
-
Bibersteinia trehalosi, serotype T4, strain S1085/81, Inactivated500000000.00/cells1.00millilitre(s)
-
Bibersteinia trehalosi, serotype T3, strain S1109/84, Inactivated500000000.00/cells1.00millilitre(s)
-
Bibersteinia trehalosi, serotype T10, strain S1075/81, Inactivated500000000.00/cells1.00millilitre(s)
-
Bibersteinia trehalosi, serotype T15, strain S1105/84, Inactivated500000000.00/cells1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI04AB05
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
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 Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Paul-Ehrlich-Institut
Authorisation number:
- 73a/97
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
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 6/02/2026