INTERMECTIN SUPER RO, 10 mg/ml + 100 mg/ml, soluție injectabilă pentru bovine
INTERMECTIN SUPER RO, 10 mg/ml + 100 mg/ml, soluție injectabilă pentru bovine
Authorised
- Ivermectin
- Clorsulon
Product identification
Medicine name:
INTERMECTIN SUPER RO, 10 mg/ml + 100 mg/ml, soluție injectabilă pentru bovine
Active substance:
- Ivermectin
- Clorsulon
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin10.00/milligram(s)1.00millilitre(s)
-
Clorsulon100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal66dayLapte: Nu se utilizează la animale în perioada de lactație sau cu 28 zile înaintea fătării, dacă laptele este destinat consumului uman.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Romania
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 18 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Lovapharm Consulting B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Interchemie Werken De Adelaar Eesti AS
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 250158
Date of authorisation status change:
Generic of:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 19/11/2025