Veterinary Medicine Information website

Cepritect 250 mg Intramammary Suspension for Dry Cows

Authorised
  • Cefalonium dihydrate
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Product identification

Medicine name:
Cepritect 250 mg Intramammary Suspension for Dry Cows
Active substance:
  • Cefalonium dihydrate
Target species:
  • Cattle
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • Cefalonium dihydrate
    269.63
    milligram(s)
    /
    1.00
    Syringe
Pharmaceutical form:
  • Intramammary suspension
Withdrawal period by route of administration:
  • Intramammary use
    • Cattle
      • Meat and offal
        21
        day
      • Milk
        96
        hour
      • Milk
        58
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ51DB90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
Package description:
  • Single dose 3g white LDPE syringes with a white LDPE dual push-fit cap.Buckets of 120 syringes including 120 individually wrapped teat cleaning towels containing isopropyl alcohol.
  • Single dose 3g white LDPE syringes with a white LDPE dual push-fit cap.Cartons of 60 syringes including 60 individually wrapped teat cleaning towels containing isopropyl alcohol.
  • Single dose 3g white LDPE syringes with a white LDPE dual push-fit cap.Cartons of 24 syringes including 24 individually wrapped teat cleaning towels containing isopropyl alcohol.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Manufacturing Limited
  • Norbrook Laboratories Limited
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 105086
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0559/001
Concerned member states:
  • Austria
  • Bulgaria
  • Czechia
  • Estonia
  • France
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Poland
  • Portugal
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 22/12/2024
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Italian (PDF)
Published on: 15/04/2022
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Summary of Product Characteristics

English (PDF)
Published on: 22/12/2024
Download