Veterinary Medicines

Uniferon 20 % w/v Solution for Injection

Authorised
  • Iron dextran
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Product identification

Medicine name:
Uniferon 20 % w/v Solution for Injection
Active substance:
  • Iron dextran
Target species:
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Iron dextran
    551.33
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        28
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QB03AC
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • Pack sizes of 5 x 100 ml multidose collapsible polyethylene vials. Vials are closed by rubberstoppers and aluminium caps. They are packed in aluminium foil.The packaging may contain an injector.
  • Pack sizes of 10 x 100 ml multidose collapsible polyethylene vials. Vials are closed by rubberstoppers and aluminium caps. They are packed in aluminium foil.The packaging may contain an injector.
  • Pack sizes of 12 x 200 ml multidose collapsible polyethylene vials. Vials are closed by rubberstoppers and aluminium caps. They are packed in aluminium foil.The packaging may contain an injector.
  • Pack sizes of 5 x 100 ml multidose collapsible polyethylene vials. Vials are closed by rubberstoppers and aluminium caps. They are packed in transparent foil.The packaging may contain an injector.
  • Pack sizes of 10 x 100 ml multidose collapsible polyethylene vials. Vials are closed by rubberstoppers and aluminium caps. They are packed in transparent foil.The packaging may contain an injector.
  • Pack sizes of 12 x 200 ml multidose collapsible polyethylene vials. Vials are closed by rubberstoppers and aluminium caps. They are packed in transparent foil.The packaging may contain an injector.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Pharmacosmos A/S
Marketing authorisation date:
Manufacturing sites for batch release:
  • Pharmacosmos A/S
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10794/001/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 25/09/2024
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