OXYTRIM prášok na perorálny roztok
OXYTRIM prášok na perorálny roztok
Authorised
- Oxytetracycline hydrochloride
- Sulfadimidine sodium
- Trimethoprim
Product identification
Medicine name:
OXYTRIM prášok na perorálny roztok
Active substance:
- Oxytetracycline hydrochloride
- Sulfadimidine sodium
- Trimethoprim
Target species:
-
Pig
-
Cattle (calf)
-
Chicken (broiler)
-
Turkey
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride40.00/milligram(s)1.00gram(s)
-
Sulfadimidine sodium50.00/milligram(s)1.00gram(s)
-
Trimethoprim10.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
In drinking water use
-
Pig
-
Meat and offal15day
-
-
Cattle (calf)
-
Meat and offal21day
-
-
Chicken (broiler)
-
Meat and offal15dayDo not use in laying hens producing eggs for human consumption
-
-
Turkey
-
Meat and offal15day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA56
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Pharmagal spol. s r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Pharmagal spol. s r.o.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/0254/97-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet