Equipalazone 1 g Oral Powder
Equipalazone 1 g Oral Powder
Authorised
- Phenylbutazone
Product identification
Medicine name:
Equipalazone 1 g Oral Powder
Active substance:
- Phenylbutazone
Target species:
-
Horse (non food-producing)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Phenylbutazone1000.00/milligram(s)1.00Sachet
Pharmaceutical form:
-
Oral powder
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Sachets of a paper/polyethylene outer layer and aluminium/polyethylene inner layer, in packs of 100 sachets (25 strips of four sachets). Each sachet contains 1.5 g Equipalazone Powder.
- Sachets of a paper/polyethylene outer layer and aluminium/polyethylene inner layer, in packs of 32 sachets (8 strips of four sachets). Each sachet contains 1.5 g Equipalazone Powder.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera d.d.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA22622/006/001
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
English (PDF)
Download Published on: 3/05/2024