TUDOMAX 10 MG/G, POWDER FOR USE IN DRINKING WATER/MILK
TUDOMAX 10 MG/G, POWDER FOR USE IN DRINKING WATER/MILK
Authorised
- Bromhexine hydrochloride
Product identification
Medicine name:
TUDOMAX 10 MG/G, POWDER FOR USE IN DRINKING WATER/MILK
TUDOMAX 10 mg/g por ivóvízbe/tejbe keveréshez
Active substance:
- Bromhexine hydrochloride
Target species:
-
Turkey
-
Pig
-
Cattle (calf)
-
Duck
-
Chicken
-
Chicken (broiler)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Bromhexine hydrochloride10.98/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
Oral use
-
Turkey
-
Meat and offal0day
-
Eggsno withdrawal periodNot for use in birds producing eggs for consumption, during and 4 weeks before the laying phase.
-
-
Pig
-
Meat and offal0day
-
-
Cattle (calf)
-
Meat and offal2day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption.
-
-
Duck
-
Meat and offal0day
-
Eggsno withdrawal periodNot for use in birds producing eggs for consumption, during and 4 weeks before the laying phase.
-
-
Chicken
-
Eggsno withdrawal periodNot for use in birds producing eggs for consumption, during and 4 weeks before the laying phase.
-
-
Chicken (broiler)
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QR05CB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Available in:
-
Hungary
Package description:
- Bag of 500 g
- Bag of 1 kg
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:
- S P Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- S P Veterinaria S.A.
Responsible authority:
- Directorate Of Veterinary Medicinal Products
Authorisation number:
- 3843/X/17 NÉBIH ÁTI
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0295/001
Concerned member states:
-
Bulgaria
-
Cyprus
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Malta
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet