Veterinary Medicines

GABBROVET MULTI 140 MG/ML SOLUTION FOR USE IN DRINKING WATER/ MILK FOR PRE-RUMINANT CATTLE AND PIGS

Authorised
  • Paromomycin sulfate
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Product identification

Medicine name:
Gabbrovet Multi 140 mg/ml solução para administração na água de bebida / leite para bovinos pré-ruminantes e suínos
GABBROVET MULTI 140 MG/ML SOLUTION FOR USE IN DRINKING WATER/ MILK FOR PRE-RUMINANT CATTLE AND PIGS
Active substance:
  • Paromomycin sulfate
Target species:
  • Cattle (calf)
  • Pig
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Paromomycin sulfate
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for use in drinking water/milk
Withdrawal period by route of administration:
  • Oral use
    • Cattle (calf)
      • Meat and offal
        20
        day
      • Meat and offal
        110
        day
    • Pig
      • Meat and offal
        3
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Portugal
Package description:
  • Cardboard box containing 1 bottle of 250 ml (HDPE/EVOH/HDPE) containing a dosing device of 30 ml
  • Cardboard box containing 1 bottle of 500 ml (HDPE/EVOH/HDPE) containing a dosing device of 30 ml
  • Cardboard box containing 1 bottle of 1 L (HDPE/EVOH/HDPE) containing a dosing device of 30 ml
  • Cardboard box containing 1 bottle of 125 ml (HDPE) containing a dosing device of 30 ml
  • Cardboard box containing 1 bottle of 250 ml (HDPE) containing a dosing device of 30 ml
  • Cardboard box containing 1 bottle of 500 ml (HDPE) containing a dosing device of 30 ml
  • Cardboard box containing 1 bottle of 1 L (HDPE)containing a dosing device of 30 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Ceva Saude Animal Produtos Farmaceuticos E Imunologicos Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 1522/01/22DFVPT
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0429/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)
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