Hypersol 500 mg/g Powder for use in Drinking water
Hypersol 500 mg/g Powder for use in Drinking water
Authorised
- Oxytetracycline hydrochloride
Product identification
Medicine name:
HYPERSOL 500 MG/G POWDER FOR USE IN DRINKING WATER
Hypersol 500 mg/g Powder for use in Drinking water
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Chicken
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Oxytetracycline hydrochloride540.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken
-
Meat and offal7day
-
Eggsno withdrawal periodDo not use in laying birds producing eggs intended for human consumption.
-
-
Pig
-
Meat and offal7day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- 1 kg jar
- 10 kg bag
- 5 kg bag
- 5 kg bucket
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:
- Huvepharma S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Huvepharma S.A.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10453/001/001
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0251/001
Concerned member states:
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 2/05/2025
How useful was this page?: