Diatrim 200 mg/ml + 40 mg/ml solution for injection for cattle, pigs, dogs and cats
Diatrim 200 mg/ml + 40 mg/ml solution for injection for cattle, pigs, dogs and cats
Authorised
- Trimethoprim
- Sulfadiazine
Product identification
Medicine name:
Diatrim 200 mg/ml + 40 mg/ml solution for injection for cattle, pigs, dogs and cats
Diatrim 200 mg/ml + 40 mg/ml solução injetável
Active substance:
- Trimethoprim
- Sulfadiazine
Target species:
-
Cattle
-
Pig
-
Dog
-
Cat
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Trimethoprim40.00milligram(s)1.00millilitre(s)
-
Sulfadiazine200.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milk48hour
-
Meat and offal12day
-
-
Pig
-
Meat and offal20day
-
-
-
Subcutaneous use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW10
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- 1 vial in a cardboard box of uncoloured glass type II filled with 250 ml with a fluoropolymer coated chlorobutyl stopper type I secured with an aluminium cap.
- 1 vial in a cardboard box of uncoloured glass type II filled with 50 ml with a fluoropolymer coated chlorobutyl stopper type I secured with an aluminium cap.
- 1 vial in a cardboard box of uncoloured glass type II filled with 100 ml with a fluoropolymer coated chlorobutyl stopper type I secured with an aluminium cap.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 1153/01/17DFVPT
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0282/001
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
France
-
Germany
-
Hungary
-
Ireland
-
Italy
-
Lithuania
-
Luxembourg
-
Poland
-
Portugal
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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