Medimec 0.5 %w/v Pour-on Solution
Medimec 0.5 %w/v Pour-on Solution
Authorised
- Ivermectin
Product identification
Medicine name:
Medimec 0.5 %w/v Pour-on Solution
Medimec 0.5 %w/v Pour-on Solution
Active substance:
- Ivermectin
Target species:
-
Cattle
Route of administration:
-
Pour-on use
Product details
Active substance and strength:
-
Ivermectin0.50/gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Pour-on solution
Withdrawal period by route of administration:
-
Pour-on use
-
Cattle
-
Meat and offal28day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- High density polyethylene container (flat bottomed flexi packs) with a 38mm tamper evident closure (2.5L).Pack size: 2.5L.
- High density polyethylene container (flat bottomed flexi packs) with a 38mm tamper evident closure (5L).Pack size: 5L.
- High density polyethylene container (flat bottomed flexi packs) with a 38mm tamper evident closure.The 1L pack will also have a dial a dose dosing cup.Pack size: 6L.The 6L consists of a 5L and 1L pack combined in one carton.
- High density polyethylene squeeze measure pour containers with child resistant closures. Pack size: 250ml.
- High density polyethylene squeeze measure pour containers with child resistant closures. Pack size: 500ml.
- High density polyethylene squeeze measure pour containers with child resistant closures. Pack size: 1L.
- High density polyethylene container (flat bottomed flexi packs) with a 38mm tamper evident closure (1L).The 1L pack will also have a dial a dose dosing cup.Pack size: 1L.
Additional information
Entitlement type:
-
Marketing Authorisation
Marketing authorisation holder:
- Chanelle Pharmaceuticals Manufacturing Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Chanelle Pharmaceuticals Manufacturing Limited
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10987/153/001
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0172/001
Concerned member states:
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024