HYDROTRIM 500 MG/G + 100 MG/G POWDER FOR USE IN DRINKING WATER/MILK FOR CATTLE, SHEEP, PIGS AND CHICKENS
HYDROTRIM 500 MG/G + 100 MG/G POWDER FOR USE IN DRINKING WATER/MILK FOR CATTLE, SHEEP, PIGS AND CHICKENS
Authorised
- Sulfadiazine sodium
- Trimethoprim
Product identification
Medicine name:
HYDROTRIM 500 MG/G + 100 MG/G POWDER FOR USE IN DRINKING WATER/MILK FOR CATTLE, SHEEP, PIGS AND CHICKENS
Hydrotrim, 500+100mg/g, Prášek pro podání v pitné vodě/mléce
Active substance:
- Sulfadiazine sodium
- Trimethoprim
Target species:
-
Chicken
-
Pig
-
Sheep (lamb)
-
Cattle (pre-ruminant)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Sulfadiazine sodium543.90milligram(s)1.00gram(s)
-
Trimethoprim100.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
Oral use
- Chicken
-
Eggsno withdrawal periodNot for use in birds producing or intended to produce eggs for human consumption
-
Meat and offal12day
-
- Pig
-
Meat and offal12day
-
- Sheep (lamb)
-
Meat and offal12day
-
- Cattle (pre-ruminant)
-
Meat and offal12day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW10
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Package description:
- 100 g pillow sachet made of polyethylene/aluminium/polyethylene terephthalate laminate.
- 1 kg resealable block -bottom zipped sachet made of polyethylene/aluminium/polyethylene terephthalate laminate.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet J.S.C.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicines
Authorisation number:
- 96/064/23-C
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0457/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
Generic of:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 13/12/2023
Labelling
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 13/12/2023
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