RILEXINE 75 mg, tabletės katėms ir šunims
RILEXINE 75 mg, tabletės katėms ir šunims
Authorised
- Cefalexin monohydrate
Product identification
Medicine name:
RILEXINE 75 mg, tabletės katėms ir šunims
Active substance:
- Cefalexin monohydrate
Target species:
-
Dog
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Cefalexin monohydrate75.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
- Dog
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01DB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
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:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- VIRBAC
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/06/1715/001-002
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
RV1715.pdf
Lithuanian (PDF)
Download Published on: 28/06/2022
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