Acticarp 50 mg/ml, Solution for Injection
Acticarp 50 mg/ml, Solution for Injection
Not authorised
- Carprofen
Product identification
Medicine name:
Acticarp 50 mg/ml, Solution for Injection
Acticarp Cattle 50 mg/ml Oplossing voor injectie
Acticarp Cattle 50 mg/ml Solution injectable
Acticarp Cattle 50 mg/ml Injektionslösung
Active substance:
- Carprofen
Target species:
-
Cattle
Route of administration:
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Carprofen50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
-
Cattle
-
Milkno withdrawal period0 hours
-
Meat and offal21day
-
-
-
Subcutaneous use
-
Cattle
-
Milkno withdrawal periodzero hours
-
Meat and offal21day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AE91
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Revoked
Authorised in:
-
Belgium
Package description:
- 50 ml amber glass (Type I) vial closed with Flurotec (coated chlorobutyl) rubber stopper and aluminium flip off. One vial in a carton box.
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:
- Fundacio Privada Dau
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V415694
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0156/001
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: 12/09/2024
Summary of Product Characteristics
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Package Leaflet
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