Veterinary Medicines

Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution

Authorised
  • Iodine (125I)
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Product identification

Medicine name:
Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution
Bovidip 2% W/V concentraat voor speendip- of sprayoplossing voor melkkoeien
Active substance:
  • Iodine (125I)
Target species:
  • Cattle
Route of administration:
  • Teat use

Product details

Active substance and strength:
  • Iodine (125I)
    2.00
    gram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Teat dip/spray solution
Withdrawal period by route of administration:
  • Teat use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG52A
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • High-density polyethylene 5 litre cans closed with high-density polyethylene screw caps,secured with a sealing ring.
  • High-density polyethylene 10 litre cans closed with high-density polyethylene screw caps,secured with a sealing ring.
  • High-density polyethylene 20 litre cans closed with high-density polyethylene screw caps,secured with a sealing ring.
  • High-density polyethylene 60 litre cans closed with high-density polyethylene screw caps,secured with a sealing ring.
  • High-density polyethylene 200 litre cans closed with high-density polyethylene screw caps,secured with a sealing ring.The 200 litre container should not be returned for re-filling.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Delaval
Marketing authorisation date:
Manufacturing sites for batch release:
  • Delaval
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 103498
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0484/001
Concerned member states:
  • Belgium
  • Netherlands
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 6/07/2025
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Dutch (PDF)
Published on: 28/07/2025
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Summary of Product Characteristics

English (PDF)
Published on: 6/07/2025
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