VETOSPIRIN 1000 mg/g powder for use in drinking water/milk
VETOSPIRIN 1000 mg/g powder for use in drinking water/milk
Authorised
- Sodium salicylate
Product identification
Medicine name:
VETOSPIRIN 1000 mg/g powder for use in drinking water/milk
Vetospirin 1000 mg/g Poeder voor toediening in het drinkwater/in de melk
Vetospirin 1000 mg/g Poudre pour administration dans le lait ou l'eau de boisson
Vetospirin 1000 mg/g Pulver zum Eingeben über das Trinkwasser/die Milch
Active substance:
- Sodium salicylate
Target species:
-
Cattle (calf)
-
Pig
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Sodium salicylate1000.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Cattle (calf)
-
Meat and offalno withdrawal period0 days
-
-
Pig
-
Meat and offalno withdrawal period0 days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02BA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- 1.0 kg multi-layered bag with an inner layer made of polyethylene
- 5.0 kg multi-layered bag with an inner layer made of polyethylene
- 10 multi-layer bags of 100 g with low density polyethylene inner layer packed in one cardboard box
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:
- V.M.D.
Marketing authorisation date:
Manufacturing sites for batch release:
- V.M.D.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0250/001
Concerned member states:
-
Belgium
-
Estonia
-
France
-
Germany
-
Hungary
-
Latvia
-
Lithuania
-
Luxembourg
-
Poland
-
Portugal
-
Romania
-
Spain
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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Combined File of all Documents
English (PDF)
Download Published on: 15/08/2025
Labelling
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