Veterinary Medicines

OXYVET 100 mg/ml solution for injection

Authorised
  • Oxytetracycline hydrochloride
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Product identification

Medicine name:
ОКСИВЕТ 100 mg/ml инжекционен разтвор
OXYVET 100 mg/ml solution for injection
Active substance:
  • Oxytetracycline hydrochloride
Target species:
  • Cattle
  • Pig
  • Sheep
  • Goat
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Intravenous 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:
  • Intramuscular use
    • Cattle
      • Meat and offal
        22
        day
      • Milk
        7
        day
    • Pig
      • Meat and offal
        22
        day
    • Sheep
      • Meat and offal
        22
        day
      • Milk
        7
        day
    • Goat
      • Meat and offal
        22
        day
      • Milk
        7
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        22
        day
      • Milk
        7
        day
      • Milk
        7
        day
    • Pig
      • Meat and offal
        22
        day
    • Sheep
      • Meat and offal
        22
        day
      • Milk
        7
        day
    • Goat
      • Meat and offal
        22
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Bulgaria
Available in:
  • Bulgaria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • PROVET S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • PROVET S.A.
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-2011
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Bulgarian (PDF)
Published on: 7/10/2025
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Package Leaflet

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Bulgarian (PDF)
Published on: 7/10/2025
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Labelling

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Bulgarian (PDF)
Published on: 7/10/2025
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