Veterinary Medicines

Terramycin LA 200 mg/ml Solution for Injection

Not authorised
  • Oxytetracycline dihydrate
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Product identification

Medicine name:
Terramycin LA 200 mg/ml Solution for Injection
Active substance:
  • Oxytetracycline dihydrate
Target species:
  • Cattle
  • Sheep
  • Deer
  • Pig
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Oxytetracycline dihydrate
    215.60
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        21
        day
      • Milk
        7
        day
    • Sheep
      • Meat and offal
        21
        day
    • Deer
      • Meat and offal
        30
        day
    • Pig
      • Meat and offal
        21
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        21
        day
      • Milk
        72
        hour
  • Subcutaneous use
    • Cattle
      • Meat and offal
        21
        day
    • Sheep
      • Meat and offal
        21
        day
    • Deer
      • Meat and offal
        30
        day
    • Pig
      • Meat and offal
        21
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Ireland
Package description:
  • Multi dose Type II amber coloured glass vial of 100 ml capacity stoppered with a red butyl rubber bung and capped with a centre tear off aluminium crimp seal and grey flick-off cap - containing a sterile, clear yellow to amber solution.

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:
  • Zoetis Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10387/077/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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