Vivitonin 50 mg film-coated tablets
Vivitonin 50 mg film-coated tablets
Authorised
- Propentofylline
Product identification
Medicine name:
Vivitonin 50 mg film-coated tablets
Active substance:
- Propentofylline
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Propentofylline50.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Film-coated tablet
Withdrawal period by route of administration:
-
Oral use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QC04AD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Blister package: PVC 250µm/Aluminium foil 20µm.One pack contains 2 blister strips of 30 tablets
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet Ges.m.b.H.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10996/127/001
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
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