Rimadyl 20 mg tablets for dogs /Rimadyl 50 mg tablets for dogs /Rimadyl 100 mg tablets for dogs
Rimadyl 20 mg tablets for dogs /Rimadyl 50 mg tablets for dogs /Rimadyl 100 mg tablets for dogs
Authorised
- Carprofen
- Carprofen
- Carprofen
Product identification
Medicine name:
Rimadyl 20 mg таблетки за кучета/Rimadyl 50 mg таблетки за кучета/Rimadyl 100 mg таблетки за кучета
Rimadyl 20 mg tablets for dogs /Rimadyl 50 mg tablets for dogs /Rimadyl 100 mg tablets for dogs
Active substance:
- Carprofen
- Carprofen
- Carprofen
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Carprofen100.00/milligram(s)1.00Tablet
-
Carprofen50.00/milligram(s)1.00Tablet
-
Carprofen20.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM01AE91
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Bulgaria
Package description:
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
- Available only in Bulgarian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Bulgarian Food Safety Authority
Authorisation number:
- 0022-1758
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
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 17/12/2024
Package Leaflet
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in another language below.
Bulgarian (PDF)
Published on: 17/12/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Bulgarian (PDF)
Published on: 17/12/2024