Imaverol 100 mg/mL, δερματικό διάλυμα, πυκνό διάλυμα για αραίωση για βοοειδή, άλογα, σκύλους
Imaverol 100 mg/mL, δερματικό διάλυμα, πυκνό διάλυμα για αραίωση για βοοειδή, άλογα, σκύλους
Authorised
- Enilconazole
Product identification
Medicine name:
Imaverol 100 mg/mL, δερματικό διάλυμα, πυκνό διάλυμα για αραίωση για βοοειδή, άλογα, σκύλους
Active substance:
- Enilconazole
Target species:
-
Cattle
-
Dog
-
Horse
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Enilconazole100.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Concentrate for cutaneous solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Cattle
-
Meat and offal0day
-
-
Dog
-
Not applicableno withdrawal period
-
-
Horse
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD01AC90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
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:
- Audevard
Marketing authorisation date:
Manufacturing sites for batch release:
- Lusomedicamenta Sociedade Tecnica Farmaceutica S.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 82146/29-07-2022/09-02-2024/K-0234301
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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