Veterinary Medicines

RISPOVAL Pasteurella

Authorised
  • Mannheimia haemolytica, serotype A1, strain NL 1009, capsular antigen
  • Mannheimia haemolytica, serotype A1, strain NL 1009, leucotoxoid
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Product identification

Medicine name:
RISPOVAL Pasteurella
Active substance:
  • Mannheimia haemolytica, serotype A1, strain NL 1009, capsular antigen
  • Mannheimia haemolytica, serotype A1, strain NL 1009, leucotoxoid
Target species:
  • Cattle
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Mannheimia haemolytica, serotype A1, strain NL 1009, capsular antigen
    345.00
    enzyme-linked immunosorbent assay unit
    /
    1.00
    Dose
  • Mannheimia haemolytica, serotype A1, strain NL 1009, leucotoxoid
    200.00
    enzyme-linked immunosorbent assay unit
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AB04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:

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 Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Paul-Ehrlich-Institut
Authorisation number:
  • 322a/94
Date of authorisation status change:

Documents

Combined File of all Documents

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German (PDF)
Published on: 31/10/2025
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