Paramectin 1% Solution for Injection
Paramectin 1% Solution for Injection
Authorised
- Ivermectin
Product identification
Medicine name:
Paramectin 1% Solution for Injection
Paramectin 1% Solução Injectável para bovinos e suínos
Active substance:
- Ivermectin
Target species:
-
Cattle
-
Pig
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Ivermectin1.00gram(s)100.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal49day
-
- Pig
-
Meat and offal18day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Package description:
- The product will be supplied in 50 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
- The product will be supplied in 100 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
- The product will be supplied in 250 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
- The product will be supplied in 500 ml volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
- The product will be supplied in 1 litre volume, presented in high density polyethylene vial with bromobutyl bung and aluminium cap.
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:
- Norbrook Laboratories Limited
Marketing authorisation date:
Manufacturing sites for batch release:
- Norbrook Laboratories Limited
- Norbrook Manufacturing Limited
Responsible authority:
- Directorate General For Food And Veterinary
Authorisation number:
- 51396
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0119/001
Concerned member states:
-
Greece
-
Italy
-
Portugal
-
Spain
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: 11/02/2022
Combined File of all Documents
This document does not exist in this language (English). You can find it in another language below.
Portuguese (PDF)
Published on: 11/04/2022
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