Nytox vet 1000 mg/g Powder for Solution for Fish Treatment in Pouch
Nytox vet 1000 mg/g Powder for Solution for Fish Treatment in Pouch
Authorised
- Tricaine mesilate
Product identification
Medicine name:
Nytox vet 1000 mg/g Powder for Solution for Fish Treatment in pouch
Nytox vet 1000 mg/g Powder for Solution for Fish Treatment in Pouch
Active substance:
- Tricaine mesilate
Target species:
-
Fish (for reproduction)
-
Ornamental fish
Route of administration:
-
Dipping
Product details
Active substance and strength:
-
Tricaine mesilate1000.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for solution for fish treatment
Withdrawal period by route of administration:
-
Dipping
-
Fish (for reproduction)
-
Fish meat70degree dayFish must not be slaughtered for human consumption during treatment. Do not use during stripping of fish eggs intended for human consumption.
-
-
Ornamental fish
-
Fish meat70degree dayFish must not be slaughtered for human consumption during treatment. Do not use during stripping of fish eggs intended for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN01AX93
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
United Kingdom (Northern Ireland)
Package description:
- 10 g heat-sealed polyvinyl-alcohol water soluble pouch contained in a sealed aluminium/polyethylene sachet. 20 sachets packed into a cardboard outer.
- 50 g heat-sealed polyvinyl-alcohol water soluble pouch contained in a sealed aluminium/polyethylene sachet. 20 sachets packed into a cardboard outer.
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:
- Naqua Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Elara Pharmaservices Europe Limited
Responsible authority:
- The Veterinary Medicines Directorate
Authorisation number:
- Vm 49507/4000
Date of authorisation status change:
Reference member state:
-
Norway
Procedure number:
- NO/V/0015/001
Concerned member states:
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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