Butazocare Flavour 1g Granules in Sachet for Horses and Ponies
Butazocare Flavour 1g Granules in Sachet for Horses and Ponies
Authorised
- Phenylbutazone
Product identification
Medicine name:
Butazocare flavour 1g granules in sachet for horses and ponies
Butazocare Flavour 1g Granules in Sachet for Horses and Ponies
Active substance:
- Phenylbutazone
Target species:
-
Horse (non food-producing)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Phenylbutazone1000.00/milligram(s)2.00gram(s)
Pharmaceutical form:
-
Granules in sachet
Withdrawal period by route of administration:
-
Oral use
-
Horse (non food-producing)
-
Meat and offalno withdrawal periodNot to be used in horses intended for human consumption. Treated horses may never be slaughtered for human consumption. The horse must have been declared as not intended for human consumption under national horse passport legislation.
-
Milkno withdrawal periodNot to be used in horses intended for human consumption. Treated horses may never be slaughtered for human consumption. The horse must have been declared as not intended for human consumption under national horse passport legislation.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
United Kingdom (Northern Ireland)
Package description:
- (ID2) 200 gram(s): unspecified outer container with 100 Bag (paper; polyethylene; aluminium; polyethylene) each with 2 gram(s)
- (ID1) 64 gram(s): unspecified outer container with 32 Bag (paper; polyethylene; aluminium; polyethylene) each with 2 gram(s)
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:
- Ecuphar
Marketing authorisation date:
Manufacturing sites for batch release:
- Labo Smeets
Responsible authority:
- The Veterinary Medicines Directorate
Authorisation number:
- Vm 32742/4026
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0332/001
Concerned member states:
-
Austria
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 7/01/2026