Solacyl 1000 mg/g powder for use in drinking water for turkeys
Solacyl 1000 mg/g powder for use in drinking water for turkeys
Authorised
- Sodium salicylate
Product identification
Medicine name:
Solacyl 1000 mg/g powder for use in drinking water for turkeys
Active substance:
- Sodium salicylate
Target species:
-
Turkey
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Sodium salicylate1000.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
In drinking water use
-
Turkey
-
Eggno withdrawal periodNot for use in birds producing or intended to produce eggs for human consumption.
-
Meat and offal2day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02BA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- (ID6) 5 kilogram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 5 kilogram(s)
- (ID5) 2.5 kilogram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 2.5 kilogram(s)
- (ID4) 1 kilogram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 1 kilogram(s)
- (ID3) 500 gram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 500 gram(s)
- (ID2) 250 gram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 250 gram(s)
- (ID1) 100 gram(s): unspecified outer container with 1 Bag (polyethylene terephthalate; aluminium; polyamide; polyethylene) with 100 gram(s)
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:
- Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402381.00.00
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0170/001
Concerned member states:
-
Czechia
-
France
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
