OXYVET 500 mg/pesariu
OXYVET 500 mg/pesariu
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
OXYVET 500 mg/pesariu
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Cattle (cow)
-
Horse (mare)
-
Pig (female)
-
Sheep (ewe)
-
Goat (adult female)
Route of administration:
-
Intrauterine use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride500.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Intrauterine tablet
Withdrawal period by route of administration:
-
Intrauterine use
-
Cattle (cow)
-
Milk48hour
-
-
Horse (mare)
-
Milk48hour
-
-
Pig (female)
-
Sheep (ewe)
-
Milk48hour
-
-
Goat (adult female)
-
Milk48hour
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG51AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Romania
Available in:
-
Romania
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- PROVET S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- PROVET S.A.
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 220114
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Romanian (PDF)
Published on: 23/08/2024
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