Marbonor 100 mg/ml Solution for Injection for cattle and pig
Marbonor 100 mg/ml Solution for Injection for cattle and pig
Authorised
- Marbofloxacin
Product identification
Medicine name:
Marbonor 100 mg/ml Solution for Injection for cattle and pig
Marbonor 100 mg/ml injekčný roztok pre hovädzí dobytok a ošípané
Active substance:
- Marbofloxacin
Target species:
-
Cattle
-
Pig
Route of administration:
-
Intramuscular use
-
Intravenous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Marbofloxacin100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Meat and offal6day
-
Milk36hour
-
- Pig
-
Meat and offal4day
-
-
Intravenous use
- Cattle
-
Meat and offal6day
-
Milk36hour
-
-
Subcutaneous use
- Cattle
-
Meat and offal6day
-
Milk36hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA93
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- The product is packaged in 60 ml amber co-ex plastic (polypropylene) vials. The vials are closed with chlorobutyl rubber stoppers sealed with aluminium caps.
- The product is packaged in 500 ml amber type II glass vials and amber co-ex plastic (polypropylene) vials. The vials are closed with chlorobutyl rubber stoppers sealed with aluminium caps.
- The product is packaged in 250 ml amber type II glass vials and amber co-ex plastic (polypropylene) vials. The vials are closed with chlorobutyl rubber stoppers sealed with aluminium caps.
- The product is packaged in 100 ml amber type II glass vials and amber co-ex plastic (polypropylene) vials. The vials are closed with chlorobutyl rubber stoppers sealed with aluminium caps.
- The product is packaged in 50 ml amber type II glass vials. The vials are closed with chlorobutyl rubber stoppers sealed with aluminium caps.
- The product is packaged in 20 ml amber type II glass vials. The vials are closed with chlorobutyl rubber stoppers sealed with aluminium caps.
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:
- Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/018/DC/13-S
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0296/001
Concerned member states:
-
Cyprus
-
Czechia
-
Estonia
-
Finland
-
Greece
-
Hungary
-
Latvia
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 10/01/2024
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