HYMATIL 300 mg/ml Solution for injection for cattle
HYMATIL 300 mg/ml Solution for injection for cattle
Authorised
- Tilmicosin
Product identification
Medicine name:
HYMATIL 300 mg/ml Solution for injection for cattle
HYMATIL 300 mg/ml raztopina za injiciranje za govedo in ovce
Active substance:
- Tilmicosin
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Tilmicosin300.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal70day
-
- Sheep
-
Meat and offal42day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01FA91
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Package description:
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
- Available only in Slovenian
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:
- Industrial Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Industrial Veterinaria S.A.
- Animedica GmbH
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- MR/V/0168/001
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0141/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
Estonia
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
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: 22/12/2023
Slovenian (PDF)
Published on: 10/06/2022
Package Leaflet
English (PDF)
Download Published on: 22/12/2023
Slovenian (PDF)
Published on: 10/06/2022
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