DAIMETON 40 soluzione iniettabile al 40% per bovini, equini, suini, polli da carne, tacchini, cani e gatti
DAIMETON 40 soluzione iniettabile al 40% per bovini, equini, suini, polli da carne, tacchini, cani e gatti
Authorised
- Sulfamonomethoxine sodium
Product identification
Medicine name:
DAIMETON 40 soluzione iniettabile al 40% per bovini, equini, suini, polli da carne, tacchini, cani e gatti
Active substance:
- Sulfamonomethoxine sodium
Target species:
-
Turkey
-
Cattle
-
Chicken (broiler)
-
Dog
-
Cat
-
Pig
-
Horse
Route of administration:
-
Intramuscular use
-
Intravenous use
Product details
Active substance and strength:
-
Sulfamonomethoxine sodium43.00gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Turkey
-
Meat and offal28dayUso non autorizzato in uccelli che producono uova per il consumo umano
-
-
Cattle
-
Milk72hour
-
Meat and offal11day
-
-
Chicken (broiler)
-
Meat and offal28dayUso non autorizzato in uccelli che producono uova per il consumo umano
-
-
Dog
-
Cat
-
Pig
-
Meat and offal16day
-
-
-
Intravenous use
-
Turkey
-
Meat and offal28dayUso non autorizzato in uccelli che producono uova per il consumo umano
-
-
Cattle
-
Milk72hour
-
Meat and offal11day
-
-
Chicken (broiler)
-
Meat and offal28dayUso non autorizzato in uccelli che producono uova per il consumo umano
-
-
Dog
-
Cat
-
Pig
-
Meat and offal16day
-
-
Horse
-
Meat and offal35dayUso non autorizzato in equidi che producono latte per il consumo umano
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EQ
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:
- Izo S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
- Izo S.r.l.
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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in another language below.
Italian (PDF)
Published on: 3/06/2022
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