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Oestrophan 0,25 mg/ml injekčný roztok

Authorised
  • Cloprostenol sodium
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Product identification

Medicine name:
Oestrophan 0,25 mg/ml injekčný roztok
Active substance:
  • Cloprostenol sodium
Target species:
  • Cattle (cow)
  • Cattle (heifer)
  • Horse (mare)
  • Pig (sow)
Route of administration:
  • Submucosal use
  • Intramuscular use

Product details

Active substance and strength:
  • Cloprostenol sodium
    263.16
    microgram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Submucosal use
    • Cattle (cow)
      • Meat
        1
        day
    • Cattle (heifer)
      • Meat
        1
        day
  • Intramuscular use
    • Cattle (cow)
      • Meat
        1
        day
    • Cattle (heifer)
      • Meat
        1
        day
    • Horse (mare)
      • Meat
        1
        day
    • Pig (sow)
      • Meat
        1
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG02AD90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Bioveta a.s.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bioveta a.s.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 99/238/80-C/S
Date of authorisation status change:

Documents

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Slovak (PDF)
Published on: 21/08/2024
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