Veterinary Medicines

RECEPTAL

Authorised
  • Buserelin acetate
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Product identification

Medicine name:
RECEPTAL
Active substance:
  • Buserelin acetate
Target species:
  • Pig (sow for reproduction)
  • Horse (mare)
  • Rabbit (female for reproduction)
  • Cattle (cow)
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Buserelin acetate
    4.20
    microgram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig (sow for reproduction)
      • Meat and offal
        0
        day
    • Horse (mare)
      • Meat and offal
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
    • Cattle (cow)
      • Meat and offal
        0
        day
  • Intravenous use
    • Pig (sow for reproduction)
      • Meat and offal
        0
        day
    • Horse (mare)
      • Meat and offal
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
    • Cattle (cow)
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Pig (sow for reproduction)
      • Meat and offal
        0
        day
    • Horse (mare)
      • Meat and offal
        0
        day
    • Rabbit (female for reproduction)
      • Meat and offal
        0
        day
    • Cattle (cow)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01CA90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Spain
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:
  • Merck Sharp & Dohme Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International GmbH
Responsible authority:
  • The Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 1106 ESP
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 8/04/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 8/04/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 8/04/2024
Download
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