Eprecis 5 mg/ml pour-on solution for cattle, sheep and goats
Eprecis 5 mg/ml pour-on solution for cattle, sheep and goats
Authorised
This information is not available for this product.
Product identification
Medicine name:
Eprecis 5 mg/ml pour-on solution for cattle, sheep and goats
Eprecis 5 mg/ml solução para unção contínua para bovinos, ovinos e caprinos
Active substance:
This information is not available for this product.
Target species:
-
Goat
-
Sheep
-
Cattle
Route of administration:
-
Pour-on use
-
Topical use
Product details
Active substance and strength:
This information is not available for this product.
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Pour-on use
- Goat
-
Meat and offal1day
-
Milk0hour
-
- Sheep
-
Meat and offal2day
-
Milk0hour
-
-
Topical 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:
-
Valid
Authorised in:
-
Portugal
Package description:
- Squeeze-measure pour-on system:250 ml translucent high density polyethylene (HDPE) bottle including 10 ml dispenser graduated each 5 ml, with removablealuminium/PE seals and PE screw cap.
- Back pack:1 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap or 1 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap included in acardboard box.
- Back pack:2.5 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap or 2.5 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap included in acardboard box.
- Back pack:5 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap or 5 L white HDPE bottles, with a removable aluminium/PE seal and a polypropylene (PP) screw cap included in acardboard 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:
- Ceva Saude Animal Produtos Farmaceuticos E Imunologicos Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 918/01/15DFVPT
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0343/001
Concerned member states:
-
Belgium
-
Denmark
-
France
-
Germany
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 28/01/2022
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