Veterinary Medicines

Dermastitis-Blocker 3 mg/ml, teat dip solution for cattle

Not authorised
  • Iodine
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Product identification

Medicine name:
Dermastitis-Blocker 3 mg/ml, teat dip solution for cattle
MAMMIT-IO
Active substance:
  • Iodine
Target species:
  • Cattle
Route of administration:
  • Teat use

Product details

Active substance and strength:
  • Iodine
    3.08
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Teat dip solution
Withdrawal period by route of administration:
  • Teat use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QD08AG03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription except for some pack sizes
Authorisation status:
  • Surrendered
Authorised in:
  • Italy
Package description:
  • (ID1): 1 unspecified outer container with 1 Canister (High Density PolyEthylene) with 4.9 litre(s) (4.9 litre(s))
  • (ID6): 1 unspecified outer container with 1 Barrel (High Density PolyEthylene) with 194.7 litre(s) (194.7 litre(s))
  • (ID4): 1 unspecified outer container with 1 Canister (High Density PolyEthylene) with 24.3 litre(s) (24.3 litre(s))
  • (ID7): 1 unspecified outer container with 1 Barrel (High Density PolyEthylene) with 973.2 litre(s) (973.2 litre(s))
  • (ID3): 1 unspecified outer container with 1 Canister (High Density PolyEthylene) with 19.5 litre(s) (19.5 litre(s))
  • (ID5): 1 unspecified outer container with 1 Canister (High Density PolyEthylene) with 58.4 litre(s) (58.4 litre(s))
  • (ID2): 1 unspecified outer container with 1 Canister (High Density PolyEthylene) with 9.7 litre(s) (9.7 litre(s))

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:
  • Ferdinand Eimermacher GmbH und Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ferdinand Eimermacher GmbH und Co. KG
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 105208
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0180/001

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 14/05/2022
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Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 3/06/2022
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