Eprivalan 5 mg/ml pour-on solution for cattle
Eprivalan 5 mg/ml pour-on solution for cattle
Not authorised
- Eprinomectin
Product identification
Medicine name:
EPRIVALAN 5 mg/ml SOLUCION PARA UNCION DORSAL CONTINUA PARA BOVINO DE CARNE Y VACAS LECHERAS
Eprivalan 5 mg/ml pour-on solution for cattle
Active substance:
- Eprinomectin
Target species:
-
Cattle
Route of administration:
-
Pour-on use
Product details
Active substance and strength:
-
Eprinomectin5.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Pour-on use
-
Cattle
-
Meat and offal15day
-
Milk0hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Revoked
Authorised in:
-
Spain
Package description:
- Back-pack (5 litre) with induction sealed tamper evident HDPE screw on cap, containing a screw on dosing devicecapable of delivering measured amounts of product.The 5 litre back-packs are designed for use with a suitable automatic dispensing gun.
- Back-pack (2.5 litre) with induction sealed tamper evident HDPE screw on cap, containing a screw on dosing devicecapable of delivering measured amounts of product.The 2.5 litre back-packs are designed for use with a suitable automaticdispensing gun.
- HDPE bottle (1 litre) with induction sealed tamper evident HDPE screw on cap, containing a screw on dosing devicecapable of delivering measured amounts of product.The 1 litre bottle uses a 50 ml dispenser (screw-on-squeeze-and-pour measuringchamber).
- HDPE bottle (250 ml) with induction sealed tamper evident HDPE screw on cap, containing a screw on dosing devicecapable of delivering measured amounts of product.The 250 ml bottle uses a 25 ml dispenser (screw-on-squeeze-and-pour measuringchamber).
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:
- Boehringer Ingelheim Animal Health Espana S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 3474 ESP
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0487/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
