Scourguard 3
Scourguard 3
Authorised
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), strain NADC 1471, Inactivated
- Bovine rotavirus A, strain Lincoln, Live
- Bovine coronavirus, strain Hansen, Live
Product identification
Medicine name:
Scourguard 3
Active substance:
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), strain NADC 1471, Inactivated
- Bovine rotavirus A, strain Lincoln, Live
- Bovine coronavirus, strain Hansen, Live
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), strain NADC 1471, Inactivated4.50/log2 antibody titre1.00Dose
-
Bovine rotavirus A, strain Lincoln, Live10000000.00/50% tissue culture infectious dose1.00Dose
-
Bovine coronavirus, strain Hansen, Live100000.00/50% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AI01
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:
- Zoetis Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Paul-Ehrlich-Institut
Authorisation number:
- 89a/82
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
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German (PDF)
Published on: 31/10/2025