Veterinary Medicines

SELEVIT, soluzione iniettabile per vitelli, vacche, agnelli, suini, cavalli

Authorised
  • Selenium
  • ALPHA-TOCOPHEROL
  • Cyanocobalamin
  • Adenosine phosphate
  • SORBITOL (E420)
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Product identification

Medicine name:
SELEVIT, soluzione iniettabile per vitelli, vacche, agnelli, suini, cavalli
Active substance:
  • Selenium
  • ALPHA-TOCOPHEROL
  • Cyanocobalamin
  • Adenosine phosphate
  • SORBITOL (E420)
Target species:
  • Cattle (calf)
  • Cattle
  • Sheep (lamb)
  • Pig
  • Horse
Route of administration:
  • Intramuscular and intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Selenium
    0.15
    milligram(s)
    /
    1.00
    millilitre(s)
  • ALPHA-TOCOPHEROL
    70.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Cyanocobalamin
    0.10
    milligram(s)
    /
    1.00
    millilitre(s)
  • Adenosine phosphate
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • SORBITOL (E420)
    50.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular and intravenous use
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal, milk
        0
        day
    • Sheep (lamb)
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal, milk
        0
        day
  • Subcutaneous use
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Cattle
      • Meat and offal, milk
        0
        day
    • Sheep (lamb)
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal, milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA11AA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
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:
  • Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 101751
Date of authorisation status change:

Documents

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Italian (PDF)
Published on: 13/07/2022
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