Rilexine 600 600 mg Tablet
Rilexine 600 600 mg Tablet
Authorised
- Cefalexin monohydrate
Product identification
Medicine name:
Rilexine 600 600 mg Tablet
Active substance:
- Cefalexin monohydrate
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Cefalexin monohydrate631.11/milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01DB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Rilexine 600 600 mg Tablet Box with 2 blisters of 7 tablets
- Rilexine 600 600 mg Tablet Box with 3 blisters of 7 tablets
- Rilexine 600 600 mg Tablet Box with 4 blisters of 7 tablets
- Rilexine 600 600 mg Tablet Box with 20 blisters of 7 tablets
- Rilexine 600 600 mg Tablet Box with 30 blisters of 7 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:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V265614
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Summary of Product Characteristics
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Labelling
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