CORTEXILINE
CORTEXILINE
Not authorised
- NEOMYCIN SULFATE
- Methylprednisolone
- Benzylpenicillin procaine monohydrate
Product identification
Medicine name:
CORTEXILINE
Active substance:
- NEOMYCIN SULFATE
- Methylprednisolone
- Benzylpenicillin procaine monohydrate
Target species:
-
Cattle
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
NEOMYCIN SULFATE169.01milligram(s)1.00millilitre(s)
-
Methylprednisolone4.00milligram(s)1.00millilitre(s)
-
Benzylpenicillin procaine monohydrate200.57milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal60day
-
Milk9day
-
-
-
Subcutaneous use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01RV01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
France
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
- FR/V/9861360 7/1985
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
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 24/03/2022
How useful was this page?: