Veterinary Medicine Information website

Engemicina 10 % LA, solução injetável para bovinos, suínos, equinos, ovinos, cães e gatos

Authorised
  • Oxytetracycline hydrochloride
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Product identification

Medicine name:
Engemicina 10 % LA, solução injetável para bovinos, suínos, equinos, ovinos, cães e gatos
Active substance:
  • Oxytetracycline hydrochloride
Target species:
  • Cattle
  • Cattle (calf)
  • Horse
  • Horse (foal)
  • Pig
  • Pig (piglet)
  • Sheep
  • Sheep (lamb)
  • Dog
  • Cat
Route of administration:
  • Intravenous use
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Oxytetracycline hydrochloride
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        35
        day
    • Cattle (calf)
      • Meat and offal
        35
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        35
        day
      • Milk
        4
        day
      • Meat and offal
        21
        day
    • Cattle (calf)
      • Meat and offal
        35
        day
      • Meat and offal
        21
        day
    • Pig
      • Meat and offal
        10
        day
    • Pig (piglet)
      • Meat and offal
        10
        day
    • Sheep
      • Meat and offal
        21
        day
      • Milk
        4
        day
    • Sheep (lamb)
      • 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:
  • Valid
Authorised in:
  • Portugal
Available in:
  • Portugal
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:
  • MSD Animal Health Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International GmbH
  • Intervet Productions S.r.l.
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 753/01/14NFVPT
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Portuguese (PDF)
Published on: 25/03/2022
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