Veterinary Medicines

BROMHEX-AIR FORTE ORAL POWDER FOR CATTLE, PIGS, CHICKENS, TURKEYS AND DUCKS

Authorised
  • Bromhexine hydrochloride
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Product identification

Medicine name:
BROMHEX-AIR FORTE ORAL POWDER FOR CATTLE, PIGS, CHICKENS, TURKEYS AND DUCKS
Bromhex-Air forte 25 mg/g proszek doustny dla bydła świń, kur, indyków i kaczek
Active substance:
  • Bromhexine hydrochloride
Target species:
  • Turkey
  • Pig
  • Duck
  • Chicken (broiler)
  • Cattle
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Bromhexine hydrochloride
    25.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • Oral use
    • Turkey
      • Meat and offal
        0
        day
      • Eggs
        no withdrawal period
    • Pig
      • Meat and offal
        0
        day
    • Duck
      • Eggs
        no withdrawal period
      • Meat and offal
        0
        day
    • Chicken (broiler)
      • Eggs
        no withdrawal period
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal
        2
        day
      • Milk
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QR05CB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Package description:
  • 1 kg Bag
  • Box of 10 containers of 100 g
  • 100 g container

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:
  • Pharmanovo Veterinaerarzneimittel GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Animed Service AG
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 3177
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0426/002
Concerned member states:
  • Germany
  • Hungary
  • Ireland
  • Italy
  • Poland
  • United Kingdom (Northern Ireland)

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 26/05/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 26/05/2022
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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.
Polish (PDF)
Published on: 4/09/2023
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