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VIRGOCILLINE, soluție injectabilă

Not authorised
  • COLISTIN SULFATE
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Product identification

Medicine name:
VIRGOCILLINE, soluție injectabilă
Active substance:
  • COLISTIN SULFATE
Target species:
  • Horse
  • Sheep
  • Pig
  • Rabbit
  • Chicken
  • Cattle
Route of administration:
  • Intramuscular use
  • Subcutaneous use
  • Intraperitoneal use

Product details

Active substance and strength:
  • COLISTIN SULFATE
    500000.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse
      • Meat and offal
        21
        day
    • Sheep
      • Milk
        2
        day
      • Meat and offal
        21
        day
    • Pig
      • Meat and offal
        21
        day
    • Rabbit
      • Meat and offal
        21
        day
    • Chicken
      • Meat and offal
        21
        day
    • Cattle
      • Milk
        2
        day
      • Meat and offal
        21
        day
  • Subcutaneous use
    • Sheep
      • Meat and offal
        21
        day
      • Milk
        2
        day
    • Pig
      • Meat and offal
        21
        day
    • Horse
      • Meat and offal
        21
        day
    • Rabbit
      • Meat and offal
        21
        day
    • Chicken
      • Meat and offal
        21
        day
    • Cattle
      • Milk
        2
        day
      • Meat and offal
        21
        day
  • Intraperitoneal use
    • Sheep
      • Meat and offal
        21
        day
      • Milk
        2
        day
    • Pig
      • Meat and offal
        21
        day
    • Horse
      • Meat and offal
        21
        day
    • Rabbit
      • Meat and offal
        21
        day
    • Chicken
      • Meat and offal
        2
        day
    • Cattle
      • Milk
        2
        day
      • Meat and offal
        21
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01XB01
Legal status of supply:
This information is not available for this product.
Authorisation status:
  • Surrendered
Authorised in:
  • Romania
Package description:

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:
  • Dopharma B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Dopharma France
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 190237
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Romanian (PDF)
Published on: 24/11/2021
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