Vetrimoxin L.A. 150 mg/ml suspension for injection for cattle and pigs
Vetrimoxin L.A. 150 mg/ml suspension for injection for cattle and pigs
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Vetrimoxin L.A. 150 mg/ml suspension for injection for cattle and pigs
Vetrimoxin L.A. 150 mg/ml Injektionssuspension für Rinder und Schweine
Active substance:
- Amoxicillin trihydrate
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Amoxicillin trihydrate172.40/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milk3day
-
Meat and offal18day
-
-
Pig
-
Meat and offal16day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- (ID4) 3000 millilitre(s): unspecified outer container with 12 Vial (Plastic) each with 250 millilitre(s)
- (ID3) 250 millilitre(s): unspecified outer container with 1 Vial (Plastic) with 250 millilitre(s)
- (ID2) 100 millilitre(s): unspecified outer container with 1 Vial (Plastic) with 100 millilitre(s)
- (ID1) 1200 millilitre(s): unspecified outer container with 12 Vial (Plastic) each with 100 millilitre(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:
- Ceva Tiergesundheit GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- CEVA SANTE ANIMALE - LIBOURNE
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 401205.00.00
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0153/001
Concerned member states:
-
Austria
-
Denmark
-
Finland
-
Iceland
-
Ireland
-
Netherlands
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (RTF)
Download Published on: 18/12/2024
Package Leaflet
English (RTF)
Download Published on: 18/12/2024
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 18/12/2024
2401205-paren-20130213.pdf
English (PDF)
Download Published on: 18/12/2024