INFUSIO HARTMANNI IMUNA

Main information

  • Trade name:
  • INFUSIO HARTMANNI IMUNA Solution for infusion
  • Pharmaceutical form:
  • Solution for infusion
  • Administration route:
  • Intravenous use
  • Units in package:
  • 20X200ML Bottle
  • Prescription type:
  • with prescription
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • INFUSIO HARTMANNI IMUNA Solution for infusion
    Czech Republic
  • Language:
  • English

Therapeutic information

  • Therapeutic area:
  • ELECTROLYTES
  • Product summary:
  • INFUSIO HARTMANNI IMUNA

Other information

Status

  • Source:
  • SUKL - Státní ústav pro kontrolu léčiv
  • Authorization status:
  • R - active MA/authorised medicinal product
  • Authorization number:
  • 76/ 383/92-S/C
  • EAN code:
  • 8585000400675
  • Last update:
  • 17-01-2018

21-11-2018

Fresenius Kabi Issues Voluntary Nationwide Recall of Sodium Chloride Injection, USP, 0.9% Due to Product Labeling Incorrectly Stating Stoppers Do Not Contain Latex

Fresenius Kabi Issues Voluntary Nationwide Recall of Sodium Chloride Injection, USP, 0.9% Due to Product Labeling Incorrectly Stating Stoppers Do Not Contain Latex

Fresenius Kabi USA is voluntarily recalling 163 lots of Sodium Chloride Injection, USP, 0.9%, 10 mL fill in a 10 mL vial and Sodium Chloride Injection, USP, 0.9%, 20 mL fill in a 20 mL vial to the user level. The product insert states that stoppers for both the 10mL and the 20mL vials do not contain natural rubber latex; the tray label for the two vial sizes and the vial label for the 20mL vial also state that the stoppers do not contain latex. The product is being recalled because the stoppers contain n...

FDA - U.S. Food and Drug Administration

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