Veterinary Medicines

Rispoval IBR-Marker InactivatumSuspension for injection for cattle

Not authorised
  • Bovine herpesvirus 1, strain Difivac gE gene-deleted, Inactivated
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Product identification

Medicine name:
Rispoval IBR-Marker InactivatumSuspension for injection for cattle
Rispoval IBR-Marker Inactivatum, суспензия за инжектиране за говеда
Active substance:
  • Bovine herpesvirus 1, strain Difivac gE gene-deleted, Inactivated
Target species:
  • Cattle
  • Cattle (for meat production)
  • Cattle (calf)
  • Cattle (heifer)
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Bovine herpesvirus 1, strain Difivac gE gene-deleted, Inactivated
    0.01
    titre
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Cattle (for meat production)
      • Meat and offal
        0
        day
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Cattle (heifer)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Bulgaria
Package description:
  • (ID3) 100 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 100 millilitre(s)
  • (ID2) 20 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 20 millilitre(s)

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 Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-1295-01.02.2010
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0021/001

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 6/04/2022
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 6/04/2022
Download

Combined File of all Documents

English (PDF)
Published on: 28/06/2024
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