Veterinary Medicines Information website

Terramycin vet. 100 mg/ml injeksjonsvæske, oppløsning til storfe, gris og sau

Not authorised
  • Oxytetracycline
Download as PDF

Product identification

Medicine name:
Terramycin vet. 100 mg/ml injeksjonsvæske, oppløsning til storfe, gris og sau
Active substance:
  • Oxytetracycline
Target species:
  • Cattle
  • Sheep
  • Pig
Route of administration:
  • Intramuscular use
  • Subcutaneous use
  • Intravenous use
  • Intrauterine use

Product details

Active substance and strength:
  • Oxytetracycline
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        3
        day
      • Meat and offal
        30
        day
    • Sheep
      • Milk
        3
        day
      • Meat and offal
        30
        day
    • Pig
      • Meat and offal
        30
        day
  • Subcutaneous use
    • Cattle
      • Milk
        3
        day
      • Meat and offal
        30
        day
    • Sheep
      • Milk
        3
        day
      • Meat and offal
        30
        day
    • Pig
      • Meat and offal
        30
        day
  • Intravenous use
    • Cattle
      • Milk
        3
        day
      • Meat and offal
        14
        day
    • Sheep
      • Milk
        3
        day
      • Meat and offal
        14
        day
    • Pig
      • Meat and offal
        14
        day
  • Intrauterine use
    • Cattle
      • Milk
        3
        day
      • Meat and offal
        6
        day
    • Sheep
      • Milk
        3
        day
      • Meat and offal
        6
        day
    • Pig
      • Meat and offal
        6
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Norway
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Zoetis Animal Health ApS
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Norwegian Medical Products Agency
Authorisation number:
  • 0000-06427
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.
Norwegian (PDF)
Published on: 23/02/2023
Download