Urilin 40 mg/ml syrup for dogs
Urilin 40 mg/ml syrup for dogs
Authorised
- Phenylpropanolamine hydrochloride
Product identification
Medicine name:
Urilin 40 mg/ml syrup for dogs
Urilin 40 mg/ml szirup kutyák részére A.U.V.
Active substance:
- Phenylpropanolamine hydrochloride
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Phenylpropanolamine hydrochloride50.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Syrup
Withdrawal period by route of administration:
-
Oral use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG04BX91
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Package description:
- 50 ml amber type III glass bottle containing 45 ml of syrup,with a low density polyethylene dropper and a polypropylene child resistant screw cap.
- 100 ml amber type III glass bottle containing 100 ml of syrup,with a low density polyethylene dropper and a polypropylene child resistant screw cap.
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:
- Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Dales Pharmaceuticals Limited
Responsible authority:
- National Food Chain Safety Office
Authorisation number:
- 2799/X/10 MgSzH ÁTI
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0510/001
Concerned member states:
-
Austria
-
Czechia
-
Denmark
-
Germany
-
Hungary
-
Italy
-
Portugal
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
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: 11/02/2022
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