BROMHEX-AIR BASIC ORAL POWDER FOR CATTLE, PIGS, CHICKENS, TURKEYS AND DUCKS
BROMHEX-AIR BASIC ORAL POWDER FOR CATTLE, PIGS, CHICKENS, TURKEYS AND DUCKS
Authorised
- Bromhexine hydrochloride
Product identification
Medicine name:
BROMHEX-AIR BASIC ORAL POWDER FOR CATTLE, PIGS, CHICKENS, TURKEYS AND DUCKS
Bromhex-air basic 10 mg/g poeder voor oraal gebruik voor runderen, varkens, kippen, kalkoenen en eenden
Active substance:
- Bromhexine hydrochloride
Target species:
-
Turkey
-
Pig
-
Duck
-
Chicken (broiler)
-
Cattle
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Bromhexine hydrochloride10.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
Oral use
-
Turkey
-
Meat and offal0day
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption during and 4 weeks before the laying period.
-
-
Pig
-
Meat and offal0day
-
-
Duck
-
Meat and offal0day
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption during and 4 weeks before the laying period.
-
-
Chicken (broiler)
-
Meat and offal0day
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption during and 4 weeks before the laying period.
-
-
Cattle
-
Meat and offal2day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QR05CB02
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
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:
-
Generic application (Article 13(1) 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:
- Medicines Evaluation Board
Authorisation number:
- REG NL 126534
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0426/001
Concerned member states:
-
Austria
-
Belgium
-
Luxembourg
-
Netherlands
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 28/03/2022