Oxyvet 50 mg/ml Roztwór do wstrzykiwań
Oxyvet 50 mg/ml Roztwór do wstrzykiwań
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
Oxyvet 50 mg/ml Roztwór do wstrzykiwań
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Sheep
-
Horse
-
Pig
-
Cattle
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Sheep
-
Meat and offal21day
-
-
Horse
-
All relevant tissuesno withdrawal periodNot to be used in horses intended for human consumption.
Treated horses may never be slaughtered for human consumption.
The horse must have been declared as not intended for human consumption under national horse passport legislation.
-
-
Pig
-
Meat and offal21day
-
-
Cattle
-
Meat and offal24day
-
-
-
Intravenous use
-
Sheep
-
Meat and offal21day
-
-
Horse
-
All relevant tissuesno withdrawal periodNot to be used in horses intended for human consumption.
Treated horses may never be slaughtered for human consumption.
The horse must have been declared as not intended for human consumption under national horse passport legislation.
-
-
Pig
-
Meat and offal21day
-
-
Cattle
-
Meat and offal24day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
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:
- Biofaktor Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Biowet Pulawy Sp. z o.o.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 0805
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.
Polish (PDF)
Published on: 2/04/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 2/04/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 11/04/2025
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