Veterinary Medicines

Carbo-Pulbit 0,40 g / g - Granulat für Tiere

Authorised
  • CHARCOAL, ACTIVATED
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Product identification

Medicine name:
Carbo-Pulbit 0,40 g / g - Granulat für Tiere
Active substance:
  • CHARCOAL, ACTIVATED
Target species:
  • Cattle
  • Chicken
  • Dog
  • Goat
  • Sheep
  • Horse
  • Cat
  • Pig
Route of administration:
  • Oral use
  • Rectal use

Product details

Active substance and strength:
  • CHARCOAL, ACTIVATED
    100.00
    gram(s)
    /
    250.00
    gram(s)
Pharmaceutical form:
  • Granules
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Chicken
      • Eggs
        0
        day
      • Meat and offal
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Pig
      • Meat and offal
        0
        day
  • Rectal use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07BA01
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
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:
  • Elanco Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pernix Pharma Kft.
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 4222
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 26/09/2024
Updated on: 22/04/2025
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 26/09/2024
Updated on: 22/04/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 26/09/2024
Updated on: 22/04/2025
Download