Egocin 20 g/100 g peroralni prašek
Egocin 20 g/100 g peroralni prašek
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
Egocin 20 g/100 g peroralni prašek
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Poultry
-
Pig
-
Cattle (calf)
-
Sheep (lamb)
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Goat (kid)
-
Trout
-
Carp
Route of administration:
-
In-feed use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride20.00/gram(s)100.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
In-feed use
-
Poultry
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Meat and offal10dayMeso in organi sesalcev in perutnine: 10 dni.
-
Eggs3dayJajca: 3 dni.
-
-
Pig
-
Meat and offal10dayMeso in organi sesalcev in perutnine: 10 dni.
-
-
Cattle (calf)
-
Meat and offal10dayMeso in organi sesalcev in perutnine: 10 dni.
-
-
Sheep (lamb)
-
Meat and offal10dayMeso in organi sesalcev in perutnine: 10 dni.
-
-
Goat (kid)
-
Meat and offal10dayMeso in organi sesalcev in perutnine: 10 dni.
-
-
Trout
-
Meat60day90 dni pri temperaturi vode do 6 ˚C.
-
Meat70day70 dni pri temperaturi vode med 6 ˚C in 12 ˚C.
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Meat60day60 dni pri temperaturi vode nad 12 ˚C.
-
-
Carp
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Meat90day90 dni pri temperaturi vode do 10 ˚C.
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Meat70day70 dni pri temperaturi vode med 10 ˚C in 20 ˚C.
-
Meat60day60 dni pri temperaturi vode nad 20 ˚C.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Available in:
-
Slovenia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0107/001
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.
Slovenian (PDF)
Published on: 9/11/2023
Updated on: 14/11/2023
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 9/11/2023
Updated on: 14/11/2023
Labelling
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 9/11/2023
Updated on: 14/11/2023