RILEXINE 200 MG/G ORAL PASTE

Not authorised

Product identification

Medicine name:

Active substance:

Target species:

Route of administration:

Active substance and strength:

Pharmaceutical form:

Anatomical therapeutic chemical veterinary (ATCvet) codes:

Legal status of supply:

Authorisation status:

Authorised in:

Package description:

Box with one aluminium sachet containing one graduated syringe of 21 g of oral paste (7 doses): each dose can treat 20 kg
Box with one aluminium sachet containing one graduated syringe of 10.5 g of oral paste (7 doses): each dose can treat 10 kg
Box with one aluminium sachet containing one graduated syringe of 4.2 g of oral paste (14 doses): each dose can treat 2 kg

Entitlement type:

Legal basis of product authorisation:

Marketing authorisation holder:

Marketing authorisation date:

Manufacturing sites for batch release:

Responsible authority:

Office For Registration Of Medicinal Products Medical Devices And Biocidal Products

Authorisation number:

Date of authorisation status change:

Reference member state:

Procedure number:

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet