Tauramox 5 mg/ml Pour-On Solution for Cattle
Tauramox 5 mg/ml Pour-On Solution for Cattle
Authorised
- Moxidectin
Product identification
Medicine name:
Tauramox 5 mg/ml Pour-On Solution for Cattle
Active substance:
- Moxidectin
Target species:
-
Cattle
Route of administration:
-
Topical use
Product details
Active substance and strength:
-
Moxidectin5.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Topical use
- Cattle
-
Meat and offal14day
-
Milk144hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
United Kingdom (Northern Ireland)
Package description:
- The product will be supplied in:1L fluorinated high density polyethylene single neck dispensers with high density polyethylene/polypropylene caps and green fluorinated high density polyethylene ball plugs.
- The product will be supplied in:250mL fluorinated high density polyethylene single neck dispensers with high density polyethylene/polypropylene caps and green fluorinated high density polyethylene ball plugs.
- The product will be supplied in:1L white fluorinated flat high density polyethylene back-packs with white polypropylene easy peel caps.
- The product will be supplied in:2.5L white fluorinated flat high density polyethylene back-packs with white polypropylene easy peel caps.
- The product will be supplied in:5L white fluorinated flat high density polyethylene back-packs with white polypropylene easy peel caps.
- The product will be supplied in:10L white high density polyethylene fluorinated jerry can with white high density polyethylene cap
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:
- Norbrook Laboratories Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- The Veterinary Medicines Directorate
Authorisation number:
- 02000/4406
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0600/001
Concerned member states:
-
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: 9/01/2024
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