Veterinary Medicines

Catosal 100 mg/ml + 0.05 mg/ml solution for injection for cattle, horses and dogs

Authorised
  • Butafosfan
  • Cyanocobalamin
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Product identification

Medicine name:
Catosal (10 g + 0,005 g )/100 ml Roztwór do wstrzykiwań
Catosal 100 mg/ml + 0.05 mg/ml solution for injection for cattle, horses and dogs
Active substance:
  • Butafosfan
  • Cyanocobalamin
Target species:
  • Cattle
  • Dog
  • Horse
Route of administration:
  • Intravenous use
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Butafosfan
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Cyanocobalamin
    0.05
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12CX99
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Package description:
  • (ID2) 250 millilitre(s): Box (board) with 1 Vial (Glass type I) with 250 millilitre(s), closed with Stopfen (chlorobutyl rubber) and Cap`` (aluminium)
  • (ID1) 100 millilitre(s): Box (board) with 1 Vial (Glass type II) with 100 millilitre(s), closed with Stopfen (chlorobutyl rubber) and Cap`` (aluminium)
  • (ID3) 50 millilitre(s): Box (board) with 1 Vial (Glass type II) with 50 millilitre(s), closed with Stopfen (chlorobutyl rubber) and Cap`` (aluminium)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Elanco Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • KVP Pharma+Veterinaer Produkte GmbH
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 0268
Date of authorisation status change:

Documents

Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 19/03/2025
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Combined File of all Documents

English (PDF)
Published on: 4/12/2025
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