Veterinary Medicines

SCOURGUARD 3

Authorised
  • Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), strain NADC 1471, Inactivated
  • Bovine rotavirus A, strain Lincoln, Live
  • Escherichia coli, serotype O101:K30 (fimbrial adhesin F5), Inactivated
  • Bovine coronavirus, strain Hansen, Live
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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
  • Escherichia coli, serotype O101:K30 (fimbrial adhesin F5), Inactivated
  • Bovine coronavirus, strain Hansen, Live
Target species:
  • Cattle (pregnant cow)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), strain NADC 1471, Inactivated
    4.50
    log2 antibody unit(s)
    /
    1.00
    Dose
  • Bovine rotavirus A, strain Lincoln, Live
    7.00
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Escherichia coli, serotype O101:K30 (fimbrial adhesin F5), Inactivated
    4.50
    log2 antibody unit(s)
    /
    1.00
    Dose
  • Bovine coronavirus, strain Hansen, Live
    5.00
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle (pregnant cow)
      • Milk
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AI01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Zoetis Italia S.r.l
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

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Italian (PDF)
Published on: 3/06/2022
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