Synulox Lactating Cow Intramammary suspension.
Synulox Lactating Cow Intramammary suspension.
Authorised
- Prednisolone
- Amoxicillin trihydrate
- Potassium clavulanate
Product identification
Medicine name:
Synulox Lactating Cow Intramammary suspension.
SYNULOX LC 260 mg intramamálna suspenzia
Active substance:
- Prednisolone
- Amoxicillin trihydrate
- Potassium clavulanate
Target species:
-
Cattle
Route of administration:
-
Intramammary use
Product details
Active substance and strength:
-
Prednisolone10.00milligram(s)1.00Syringe
-
Amoxicillin trihydrate200.00milligram(s)1.00Syringe
-
Potassium clavulanate59.56milligram(s)1.00Syringe
Pharmaceutical form:
-
Intramammary suspension
Withdrawal period by route of administration:
-
Intramammary use
- Cattle
-
Milk60hour
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ51RV01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Package description:
- Low density polyethylene syringes packed in cartons containing 12 syringes.
- Low density polyethylene syringes packed in cartons containing 24 syringes.
- Low density polyethylene syringes packed in cartons containing 300 syringes.
- Low density polyethylene syringes packed in cartons containing 3 syringes.
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:
- Zoetis Ceska Republika s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Haupt Pharma Latina S.r.l.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/066/93-S
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0605/001
Concerned member states:
-
Austria
-
Bulgaria
-
Cyprus
-
Czechia
-
France
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024
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: 18/07/2023
Updated on: 19/07/2023
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