Kaltetan forte, 458.4 mg/ml + 125 mg/ml + 20 mg/ml solution for infusion for horses, cattle and pigs
  • CALCIUM GLUCONATE FOR INJECTION
  • Magnesiumchlorid-Hexahydrat
  • Dinātrija-1-glicerofosfāta pentahidrāts
  • Valid
Authorised in these countries:
  • Czechia
Export to PDF

Product identification

Medicine name:
Kaltetan forte, 458.4 mg/ml + 125 mg/ml + 20 mg/ml solution for infusion for horses, cattle and pigs
Kaltetan forte, 458.4+125+20mg/ml, Injekční roztok
Active substance and strength:
  • CALCIUM GLUCONATE FOR INJECTION
  • Magnesiumchlorid-Hexahydrat
  • Dinātrija-1-glicerofosfāta pentahidrāts
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12AX
Authorisation number:
  • 96/003/22-C
Product identification number:
  • e6c72c0c-7e91-4ca3-a324-f66e3938784b
Permanent identification number:
  • 600000092623

Product details

Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
  • Solution for infusion
Withdrawal period by route of administration:
  • Intravenous use
    • Horse
      • Milk
        5
        week
    • Cattle
      • Meat and offal
        5
        week
    • Pig
      • Meat and offal
        5
        week

Availability

Package description:
  • Polypropylene (PP) bottles closed with a bromobutyl rubber stopper, type I and secured with an aluminium cap. Package size: 500 ml
Manufacturing sites for batch release:
  • Vet-Agro Multi-Trade Company Sp. z o.o.
  • Vet-Agro Multi-Trade Company Sp. z o.o.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • PL/V/0110/002
Date of authorisation status change:
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Authorisation country:
  • Czechia
Responsible authority:
  • USKVBL
Marketing authorisation holder:
  • Vet-Agro Sp. z o.o.
Marketing authorisation issued:
Reference member state:
  • Poland
Concerned member states:
  • Bulgaria
  • Czechia
  • Greece
  • Hungary
  • Italy
  • Lithuania
  • Portugal
  • Romania
  • Spain
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Summary of Product Characteristics (PDF)
First published:
Last updated:
Package Leaflet (PDF)
First published:
Last updated:
Labelling (PDF)
First published:
Last updated:
Labelling (PDF)
First published:
Last updated:
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."