Parafend 2.265 % Oral Suspension
Parafend 2.265 % Oral Suspension
Authorised
- Oxfendazole
Product identification
Medicine name:
Parafend 2.265 % Oral Suspension
Active substance:
- Oxfendazole
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Oxfendazole2.27/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal14day
-
Milk5day
-
-
Sheep
-
Meat and offal10day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AC02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Parafend will be presented in 10 L multi-dose polyethylene containers with polyethylene closures.
- Parafend will be presented in 5 L multi-dose polyethylene containers with polyethylene closures.
- Parafend will be presented in 2.5 L multi-dose polyethylene containers with polyethylene closures.
- Parafend will be presented in 1.0 L multi-dose polyethylene containers with polyethylene closures.
- Parafend will be presented in 500 ml multi-dose polyethylene containers with polyethylene closures.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent (abridged application) - Council Directive 81/851/EEC
Marketing authorisation holder:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA22664/040/001
Date of authorisation status change:
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: 3/05/2024