Oxymed 500 mg/g Proszek do sporządzania roztworu doustnego
Oxymed 500 mg/g Proszek do sporządzania roztworu doustnego
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
Oxymed 500 mg/g Proszek do sporządzania roztworu doustnego
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Chicken (hen)
-
Pig
-
Cattle
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken (hen)
-
Meat and offal15day
-
-
Pig
-
Meat and offal15day
-
-
Cattle
-
Meat and offal28day
-
-
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:
- Dopharma B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma B.V.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 1483
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 8/08/2025
Summary of Product Characteristics
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in another language below.
Polish (PDF)
Published on: 8/08/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 8/08/2025