Prazil N Orale 200 mg/ml + 40 mg/ml, soluzione orale per bovini, suini, broilers, tacchini e conigli
Prazil N Orale 200 mg/ml + 40 mg/ml, soluzione orale per bovini, suini, broilers, tacchini e conigli
Authorised
- Sulfadimethoxine
- Trimethoprim
Product identification
Medicine name:
Prazil N Orale 200 mg/ml + 40 mg/ml, soluzione orale per bovini, suini, broilers, tacchini e conigli
Active substance:
- Sulfadimethoxine
- Trimethoprim
Target species:
-
Cattle (calf)
-
Pig
-
Pig (for fattening)
-
Turkey
-
Chicken (broiler)
-
Rabbit
Route of administration:
-
In drinking water/milk use
-
In drinking water use
Product details
Active substance and strength:
-
Sulfadimethoxine20.00/gram(s)100.00millilitre(s)
-
Trimethoprim4.00/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Oral solution
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Cattle (calf)
-
Meat and offal20dayUso non autorizzato in uccelli che producono uova per consumo umano
-
-
Pig
-
Meat and offal8dayUso non autorizzato in uccelli che producono uova per consumo umano
-
-
Pig (for fattening)
-
Meat and offal8dayUso non autorizzato in uccelli che producono uova per consumo umano
-
-
-
In drinking water use
-
Turkey
-
Meat and offal9dayUso non autorizzato in uccelli che producono uova per consumo umano
-
-
Chicken (broiler)
-
Meat and offal4dayUso non autorizzato in uccelli che producono uova per consumo umano
-
-
Rabbit
-
Meat and offal6dayUso non autorizzato in uccelli che producono uova per consumo umano
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW09
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
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:
- Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
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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Italian (PDF)
Published on: 13/07/2023
Updated on: 19/07/2023
