Branzil Vet. oralt pulver 1000 mg/g
Branzil Vet. oralt pulver 1000 mg/g
Authorised
- Oxolinic acid
- Oxolinic acid
Product identification
Medicine name:
Branzil Vet. oralt pulver 1000 mg/g
Active substance:
- Oxolinic acid
- Oxolinic acid
Target species:
-
Aquaculture animals
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Oxolinic acid1000.00/milligram(s)1.00gram(s)
-
Oxolinic acid1000.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MB05
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Aller Aqua A/S
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetrepharm ApS
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 39702
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Danish (, ORALT PULVER 1000 MG-G)
Published on: 29/06/2023