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 pó para administração na água de bebida
Active substance:
- Oxytetracycline hydrochloride
Target species:
-
Chicken
-
Pig
Route of administration:
-
Oral 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:
-
Oral 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:
-
Portugal
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
Marketing authorisation date:
Manufacturing sites for batch release:
- Huvepharma
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 637/01/13RFVPT
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
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Portuguese (PDF)
Published on: 13/04/2022
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