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Veterinary Medicines

INGRAVIDA, 0,0040 mg/ml soluzione iniettabile per bovine, cavalle, coniglie, scrofette e trote

Authorised
  • Buserelin acetate

Product identification

Medicine name:
INGRAVIDA, 0,0040 mg/ml soluzione iniettabile per bovine, cavalle, coniglie, scrofette e trote
Active substance:
  • Buserelin acetate
Target species:
  • Trout - Golden/Rainbow/Redband/Steelhead
  • Cattle (cow)
  • Horse (mare)
  • Rabbit (female for reproduction)
  • Pig (young female)
Route of administration:
  • Top-dressing use
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Buserelin acetate
    0.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Top-dressing use
    • Trout - Golden/Rainbow/Redband/Steelhead
      • Unspecified
        0
        day
  • Intramuscular use
    • Cattle (cow)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse (mare)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
    • Pig (young female)
      • Meat and offal
        0
        day
  • Intravenous use
    • Cattle (cow)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse (mare)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
    • Pig (young female)
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle (cow)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse (mare)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01CA90
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
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:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

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Italian (PDF)
Published on: 3/06/2022
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