Veterinary Medicines

RUVAX

Not authorised
  • Erysipelothrix rhusiopathiae, serotype 2, strain IM 950, Inactivated
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Product identification

Medicine name:
RUVAX
Active substance:
  • Erysipelothrix rhusiopathiae, serotype 2, strain IM 950, Inactivated
Target species:
  • Pig
  • Sheep (pregnant ewe)
  • Turkey (for reproduction)
  • Pig (female)
  • Pig (male for reproduction)
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Erysipelothrix rhusiopathiae, serotype 2, strain IM 950, Inactivated
    1.00
    enzyme-linked immunosorbent assay unit
    /
    1.00
    Dose
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        0
        day
    • Sheep (pregnant ewe)
      • Meat and offal
        0
        day
    • Turkey (for reproduction)
      • Meat and offal
        0
        day
    • Pig (female)
      • Meat and offal
        0
        day
    • Pig (male for reproduction)
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Pig
      • Meat and offal
        0
        day
    • Sheep (pregnant ewe)
      • Meat and offal
        0
        day
    • Turkey (for reproduction)
      • Meat and offal
        0
        day
    • Pig (female)
      • Meat and offal
        0
        day
    • Pig (male for reproduction)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI09AB03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Spain
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Boehringer Ingelheim Animal Health Espana S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Spanish Agency For Medicines And Health Products
Authorisation number:
  • 2524 ESP
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 9/11/2022
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Labelling

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Spanish (PDF)
Published on: 9/11/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 9/11/2022
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