Kelamoxil LA 150 mg/ml suspension for injection for cattle and pig
Kelamoxil LA 150 mg/ml suspension for injection for cattle and pig
Authorised
- Amoxicillin
Product identification
Medicine name:
Kelamoxil LA 150 mg/ml suspension for injection for cattle and pig
Kelamoxil LA 150 mg/ml suspensija injekcijām liellopiem un cūkām
Active substance:
- Amoxicillin
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Amoxicillin150.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal18day
-
Milk72hour
-
-
Pig
-
Meat and offal20day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Kela Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/DCP/23/0021
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0390/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
Generic of:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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