Actikor 5 mg Film-coated Tablets for Dogs
Actikor 5 mg Film-coated Tablets for Dogs
Not authorised
- Benazepril hydrochloride
- Benazepril hydrochloride
Product identification
Medicine name:
Actikor 5 mg Film-coated Tablets for Dogs
Active substance:
- Benazepril hydrochloride
- Benazepril hydrochloride
Target species:
-
Dog
-
Dog
Route of administration:
-
Oral use
-
Oral use
Product details
Active substance and strength:
-
Benazepril hydrochloride5.00milligram(s)1.00Tablet
-
Benazepril hydrochloride5.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Film-coated tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
-
Oral use
-
Dog
-
Not applicableno withdrawal periodnot applicable
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QC09AA07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Netherlands
Package description:
- 84 tablets in aluminium foil blister packs
- 56 tablets in aluminium foil blister packs
- 28 tablets in aluminium foil blister packs
- 140 tablets in aluminium foil blister packs
- 14 tablets in aluminium foil blister packs
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:
- Animalcare Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Accord Healthcare Limited
- Ecuphar
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- 107544
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0151/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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