Veterinary Medicines

Animedazon Spray, 2.45 % w/w cutaneous spray suspension for cattle, sheep and pigs

Authorised
  • Chlortetracycline hydrochloride
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Product identification

Medicine name:
Animedazon Spray, 2.45 % w/w cutaneous spray suspension for cattle, sheep and pigs
ANIMEDAZON 2,45 % w/w dermalno pršilo, suspenzija za govedo, ovce in prašiče
Active substance:
  • Chlortetracycline hydrochloride
Target species:
  • Cattle
  • Sheep
  • Pig
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Chlortetracycline hydrochloride
    3.21
    gram(s)
    /
    1.00
    Cylinder
Pharmaceutical form:
  • Cutaneous spray, suspension
Withdrawal period by route of administration:
  • Cutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QD06AA02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovenia
Available in:
  • Slovenia
Package description:
  • (ID2) 12 Cutaneous spray, suspension: unspecified outer container with 12 Cylinder each with 1 Cutaneous spray, suspension
  • (ID1) 1 Cutaneous spray, suspension: unspecified outer container with 1 Cylinder with 1 Cutaneous spray, suspension

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • aniMedica GmbH
Responsible authority:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • MR/V/0510/001
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0120/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • France
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 14/02/2022
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Slovenian (PDF)
Published on: 31/05/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 31/05/2024
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 31/05/2024
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Combined File of all Documents

English (PDF)
Published on: 30/01/2024
Download
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