Doramax 10 mg/ml Solution for Injection for Cattle, Sheep and Pigs
Doramax 10 mg/ml Solution for Injection for Cattle, Sheep and Pigs
Authorised
- Doramectin
Product identification
Medicine name:
Doramax 10 mg/ml Solution for Injection for Cattle, Sheep and Pigs
Dectomax 10 mg/ml Injektionslösung Rinder, Schafe, Schweine
Active substance:
- Doramectin
Target species:
-
Sheep
-
Pig
-
Cattle
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Doramectin10.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal70day
-
-
Pig
-
Meat and offal77day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal70day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- Type II amber glass multi-dose vials, with chlorobutyl rubber stoppers secured with an aluminium cap. Package sizes: Cardboard box containing 1 vial of 500 ml.
- Type II amber glass multi-dose vials, with chlorobutyl rubber stoppers secured with an aluminium cap. Package sizes: Cardboard box containing 1 vial of 250 ml.
- Type II amber glass multi-dose vials, with chlorobutyl rubber stoppers secured with an aluminium cap. Package sizes: Cardboard box containing 1 vial of 50 ml.
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:
- Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- V7006074.00.00
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0770/001
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
Denmark
-
France
-
Germany
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
How useful was this page?: