Enroxil Max, 100 mg/mL, otopina za injekciju
Enroxil Max, 100 mg/mL, otopina za injekciju
Authorised
- Enrofloxacin
Product identification
Medicine name:
Enroxil Max, 100 mg/mL, otopina za injekciju
Active substance:
- Enrofloxacin
Target species:
-
Pig
-
Cattle
Route of administration:
-
Intramuscular use
-
Subcutaneous use
-
Intravenous use
Product details
Active substance and strength:
-
Enrofloxacin100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Pig
-
Meat and offal12day
-
-
-
Subcutaneous use
-
Cattle
-
Meat and offal14day
-
Milk120hour
-
-
-
Intravenous use
-
Cattle
-
Meat and offal7day
-
Milk72hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Croatia
Package description:
- Available only in Croatian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Krka-Farma d.o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
- Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
- UP/I-322-05/20-01/282
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.
Croatian (PDF)
Published on: 31/07/2023
Updated on: 1/08/2023
How useful was this page?: