Pergoquin, 1 mg tablets for horses
Pergoquin, 1 mg tablets for horses
Authorised
- Pergolide mesilate
Product identification
Medicine name:
Pergoquin, 1 mg tablets for horses
Pergoquin 1 mg Tabletten für Pferde
Active substance:
- Pergolide mesilate
Target species:
-
Horse
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Pergolide mesilate1.31milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Horse
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN04BC02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- Cardboard box of 200 tablets containing Aluminium-OPA, Aluminium, PVC blisters containing 10 tablets.
- Cardboard box of 160 tablets containing Aluminium-OPA, Aluminium, PVC blisters containing 10 tablets.
- Cardboard box of 150 tablets containing Aluminium-OPA, Aluminium, PVC blisters containing 10 tablets.
- Cardboard box of 100 tablets containing Aluminium-OPA, Aluminium, PVC blisters containing 10 tablets.
- Cardboard box of 50 tablets containing Aluminium-OPA, Aluminium, PVC blisters containing 10 tablets.
- Cardboard box of 60 tablets containing Aluminium-OPA, Aluminium, PVC blisters containing 10 tablets.
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:
- Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Marketing authorisation date:
Manufacturing sites for batch release:
- Lely Pharma B.V.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402629.00.00
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0295/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
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: 9/10/2023
Updated on: 10/10/2023
German (PDF)
Published on: 20/12/2024
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