COBACTAN LA 7.5% w/v suspension for injection for cattle
COBACTAN LA 7.5% w/v suspension for injection for cattle
Not authorised
- Cefquinome sulfate
Product identification
Medicine name:
COBACTAN LA 7.5% w/v suspension for injection for cattle
Active substance:
- Cefquinome sulfate
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Cefquinome sulfate88.90/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal13day
-
Milkno withdrawal periodDo not use in dairy cows producing milk for human consumption (during lactation or the dry period). Do not use within two months prior to first calving in heifers intended for the production of milk for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01DE90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
France
Package description:
- (ID3) 50 millilitre(s): unspecified outer container with 1 Vial (Glass) with 50 millilitre(s)
- (ID2) 250 millilitre(s): unspecified outer container with 1 Vial (Glass) with 250 millilitre(s)
- (ID1) 100 millilitre(s): unspecified outer container with 1 Vial (Glass) with 100 millilitre(s)
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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International GmbH
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/5940522 1/2006
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0145/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 13/11/2023
Updated on: 14/03/2026
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 14/03/2026
