Baycox Sheep, 50 mg/ml oral suspension
Baycox Sheep, 50 mg/ml oral suspension
Not authorised
- TOLTRAZURIL
Product identification
Medicine name:
Baycox Sheep, 50 mg/ml oral suspension
Baycox Sheep vet. 50 mg/ml Mixtúra, dreifa Sauðfé (lömb)
Active substance:
- TOLTRAZURIL
Target species:
-
Sheep
-
Sheep (lamb)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
TOLTRAZURIL50.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral suspension
Withdrawal period by route of administration:
-
Oral use
-
Sheep
-
Meat and offal42dayNot authorised for use in lactating sheep producing milk for human consumption.
-
-
Sheep (lamb)
-
Meat and offal42dayNot authorised for use in lactating sheep producing milk for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP51AJ01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Iceland
Package description:
- High density polyethylene bottles containing a white or yellowish suspension with a green polypropylene screw cap for the 250 ml and 1000 ml bottle.
- High density polyethylene bottles containing a white or yellowish suspension with a green polypropylene screw cap for the 250 ml and 1000 ml bottle.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Elanco Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Elanco Animal Health GmbH
Responsible authority:
- Icelandic Medicines Agency
Authorisation number:
- IS/2/08/012/01
Date of authorisation status change:
Reference member state:
-
Norway
Procedure number:
- NO/V/002/001
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: 14/01/2022
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