Animedazon Spray, 2.45 % w/w cutaneous spray suspension for cattle, sheep and pigs
Animedazon Spray, 2.45 % w/w cutaneous spray suspension for cattle, sheep and pigs
Authorised
- Chlortetracycline hydrochloride
Product identification
Medicine name:
Animedazon Spray, 2.45 % w/w cutaneous spray suspension for cattle, sheep and pigs
Animedazon Spray 2.45 % w/w Huidspray, suspensie
Animedazon Spray 2.45 % w/w Suspension pour pulvérisation cutanée
Animedazon Spray 2.45 % w/w Spray zur Anwendung auf der Haut, Suspension
Active substance:
- Chlortetracycline hydrochloride
Target species:
-
Cattle
-
Sheep
-
Pig
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Chlortetracycline hydrochloride3.21/gram(s)1.00Cylinder
Pharmaceutical form:
-
Cutaneous spray, suspension
Withdrawal period by route of administration:
-
Cutaneous use
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD06AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- (ID2) 12 Cutaneous spray, suspension: unspecified outer container with 12 Cylinder each with 1 Cutaneous spray, suspension
- (ID1) 1 Cutaneous spray, suspension: unspecified outer container with 1 Cylinder with 1 Cutaneous spray, suspension
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:
- aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- aniMedica GmbH
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V503191
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0120/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
France
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Labelling
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