Veterinary Medicines

Paramectin 1% Solution for Injection

Not authorised
  • Ivermectin
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Product identification

Medicine name:
Paramectin 1% Solution for Injection
Paramectin 10mg/ml ενέσιμο διάλυμα για βοοειδή και χοίρους
Active substance:
  • Ivermectin
Target species:
  • Cattle
  • Pig
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Ivermectin
    1.00
    gram(s)
    /
    100.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        49
        day
    • Pig
      • Meat and offal
        18
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QP54AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Greece
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 (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Manufacturing Limited
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 67191/17-10-2008/Κ-0141801
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0119/001

Documents

Summary of Product Characteristics

English (PDF)
Published on: 29/12/2024
Download

Combined File of all Documents

English (PDF)
Published on: 29/12/2024
Download
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