Veterinary Medicines

Bovifer, 200 mg/ml, solution for injection

Authorised
  • IRON(III)-HYDROXIDE DEXTRAN COMPLEX
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Product identification

Medicine name:
Bovifer, 200 mg/ml, solution for injection
Bovifer 200 mg/ml, oplossing voor injectie voor runderen (kalveren)
Active substance:
  • IRON(III)-HYDROXIDE DEXTRAN COMPLEX
Target species:
  • Cattle (calf)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • IRON(III)-HYDROXIDE DEXTRAN COMPLEX
    519.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle (calf)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB03AC
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • Carton box with 5 vials (LDPE) with 200 ml
  • Carton box with 48 vials (LDPE) with 100 ml
  • Carton box with 20 vials (LDPE) with 100 ml
  • Carton box with 12 vials (LDPE) with 200 ml
  • Carton box with 12 vials (LDPE) with 100 ml
  • Carton box with 10 vials (LDPE) with 100 ml
  • Carton box with 1 vial (LDPE) with 200 ml
  • Carton box with 1 vial (LDPE) with 100 ml
  • Carton box with 5 vials (LDPE) with 100 ml
  • Carton box with 5 vials (glass) with 100 ml
  • Carton box with 48 vials (glass) with 100 ml
  • Carton box with 20 vials (glass) with 100 ml
  • Carton box with 12 vials (glass) with 100 ml
  • Carton box with 10 vials (glass) with 100 ml
  • Carton box with 1 vial (glass) with 100 ml

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
  • Pharmacosmos A/S
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pharmacosmos A/S
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 131069
Date of authorisation status change:
Reference member state:
  • Sweden
Procedure number:
  • SE/V/0124/001
Concerned member states:
  • Belgium
  • Denmark
  • France
  • Germany
  • Ireland
  • Italy
  • Netherlands
  • Poland
  • Spain

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 21/01/2025
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Summary of Product Characteristics

English (PDF)
Published on: 3/03/2025
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Package Leaflet

English (PDF)
Published on: 3/03/2025
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Labelling

English (PDF)
Published on: 3/03/2025
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eu-puar-sev01240001-mr-bovifer-solution-for-injection-en.pdf

English (PDF)
Published on: 6/03/2025
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