Zerofen 25 mg/ml Oral Suspension
Zerofen 25 mg/ml Oral Suspension
Authorised
- Fenbendazole
Product identification
Medicine name:
Zerofen 25 mg/ml Oral Suspension
Active substance:
- Fenbendazole
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Fenbendazole2.50/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal14day
-
Milk96hour
-
-
Sheep
-
Meat and offal21day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP52AC13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- A suspension contained in 10 L high density polythene containers with polypropylene closures.
- A suspension contained in 5 L high density polythene containers with polypropylene closures.
- A suspension contained in 2.5 high density polythene containers with polypropylene closures.
- A suspension contained in 1 L high density polythene containers with polypropylene closures.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed consent application (Article 13c of Directive No 2001/82/EC)
Marketing authorisation holder:
- Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10987/017/002
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: 25/09/2024