Pharmasin 1 g/g granules for use in drinking water for pigs, chickens, turkeys and calves
Pharmasin 1 g/g granules for use in drinking water for pigs, chickens, turkeys and calves
Authorised
- Tylosin tartrate
Product identification
Medicine name:
Pharmasin 1 g/g granules for use in drinking water for pigs, chickens, turkeys and calves
Active substance:
- Tylosin tartrate
Target species:
-
Pig
-
Chicken
-
Cattle (calf)
-
Turkey
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Tylosin tartrate1100.00/milligram(s)1.10gram(s)
Pharmaceutical form:
-
Granules for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Pig
-
Meat and offal1day
-
-
Chicken
-
Meat and offal1day
-
Eggsno withdrawal periodzero days
-
-
Cattle (calf)
-
Meat and offal12day
-
-
Turkey
-
Meat and offal2day
-
Eggsno withdrawal periodzero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01FA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Available in:
-
Netherlands
Package description:
- 1.1 kg resealable block bottom zipped sachet made of polyethylene /aluminium/polyethylene terephthalate laminate.
- 110 g high density polyethylene pot with polypropylene cap.
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:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet AD
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 107365
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0159/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Denmark
-
Germany
-
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
Documents
Combined File of all Documents
English (PDF)
Download Published on: 9/11/2023
Updated on: 14/11/2023
Dutch (PDF)
Published on: 14/11/2023
Updated on: 15/11/2023