Vulketan 2.5 mg/g Gel
Vulketan 2.5 mg/g Gel
Authorised
- Ketanserin tartrate
Product identification
Medicine name:
Vulketan 2.5 mg/g Gel
Vulketan 2.5 mg/g Gel
Vulketan 2.5 mg/g Gel
Active substance:
- Ketanserin tartrate
Target species:
-
Horse
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Ketanserin tartrate3.45/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Gel
Withdrawal period by route of administration:
-
Cutaneous use
- Horse
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD03AX90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Vulketan Tube with 75 g Gel
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Audevard
Marketing authorisation date:
Manufacturing sites for batch release:
- Sanochemia Pharmazeutika AG
Responsible authority:
- FAMHP
Authorisation number:
- BE-V155242
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Summary of Product Characteristics
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