Gabbrovet 140 140 mg/g Poeder voor toediening in het drinkwater/in de melk
Gabbrovet 140 140 mg/g Poeder voor toediening in het drinkwater/in de melk
Authorised
- Paromomycin
Product identification
Medicine name:
Gabbrovet 140 140 mg/g Poeder voor toediening in het drinkwater/in de melk
Gabbrovet 140 140 mg/g Poudre pour administration dans le lait ou l'eau de boisson
Gabbrovet 140 140 mg/g Pulver zum Eingeben über das Trinkwasser/die Milch
Active substance:
- Paromomycin
Target species:
-
Cattle (pre-ruminant)
-
Pig
Route of administration:
-
In drinking water/milk use
-
In drinking water use
Product details
Active substance and strength:
-
Paromomycin140.00milligram(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 (pre-ruminant)
-
Meat and offal20day
-
-
In drinking water use
- Pig
-
Meat and offal3day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Gabbrovet 140 1 kg Jar Powder for use in drinking water/milk
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Unione Commerciale Lombarda S.p.A.
- Ceva Vetem S.p.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V131616
Date of authorisation status change:
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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