TRICHOLOR
TRICHOLOR
Authorised
- Trichophyton verrucosum, strain LTF-130, Live
Product identification
Medicine name:
TRICHOLOR
Active substance:
- Trichophyton verrucosum, strain LTF-130, Live
Target species:
-
Cattle
-
Cattle (pre-ruminant)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Trichophyton verrucosum, strain LTF-130, Live60000000.00/Colony forming unit1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal7day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AP01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
France
Package description:
- 1 Box with (1 Bottle (Glass) with 20 vaccine doses and 1 Bottle (Glass) with 40 millilitres) (20 ID, 40 ml)
- 1 Box with (1 Bottle (Glass) with 10 vaccine doses and 1 Bottle (Glass) with 20 millilitres) (10 ID, 20 ml)
- 1 Box with (1 Bottle (Glass) with 5 vaccine doses and 1 Bottle (Glass) with 10 millilitres) (5 ID, 10 ml)
- 1 Box with (1 Bottle (Glass) with 40 vaccine doses and 1 Bottle (Glass) with 40 millilitres) (40 ID, 40 ml)
- 1 Box with (1 Bottle (Glass) with 20 vaccine doses and 1 Bottle (Glass) with 20 millilitres) (20 ID, 20 ml)
- 1 Box with (1 Bottle (Glass) with 10 vaccine doses and 1 Bottle (Glass) with 10 millilitres) (10 ID, 10 ml)
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:
- Ceva Tiergesundheit (Riems) GmbH
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/7342461 1/2022
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0293/001
Concerned member states:
-
France
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet and Labelling
This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 15/10/2025
Package Leaflet
English (PDF)
Download Published on: 13/03/2026
English (PDF)
Published on: 4/09/2023
Updated on: 14/03/2026
7007814-paren-20230817.pdf
English (PDF)
Download Published on: 13/03/2026