01 12Care4 Aps
02 12care4 ApS
03 1Central Procurement & Supplies Unit
04 1Hospira UK Limited
05 1Medartuum Ab
06 1NORIDEM ENTERPRISES LTD
07 1NOVARTIS FARMA SPA
08 1Novartis Healthcare A/S
09 1Novartis Ireland Limited
10 1Novartis Norway (2)
11 1Novartis Pharma Schweiz Ag
12 1Novartis Pharmaceuticals Sa
13 1Novartis Sweden Ab
14 2Olon Spa
15 1Orifarm A/S
16 3Orifarm Ab
17 2Paranova Pharmaceuticals Ab
18 1Pharmachim Ab
01 5Deferoxamine
02 14Deferoxamine Mesylate
03 2Deferoxamine mesylate
04 1deferoxamine
01 14Injection/Infusion Solution
02 2Lyophilizate
03 1Powder And Solvent For Injection
04 1Powder For Injection Or Infusion Solution
05 2Powder For Solution For Injection
06 1Powder For Solution For Injection And Infusion
07 1Solution For Injection
01 3Denmark
02 4Italy
03 3Malta
04 2Norway
05 1Spain
06 8Sweden
07 1Switzerland
01 1DEFEROXAMINA NORIDEM
02 1DESFERAL
03 1Deferoxamine Mesylate "Orifarm"
04 13Desferal
05 1Desferal Vials,
06 2Desferin
07 1Desferrioxamine Mesilate
08 2Blank
Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Desferal
Dosage Form : Injection/Infusion Solution
Dosage Strength : 500mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Prescription
Registration Country : Denmark
Brand Name : Desferal
Dosage Form : Injection/Infusion Solution
Dosage Strength : 500mg
Packaging :
Approval Date : 14-02-2012
Application Number : 28105009212
Regulatory Info : Prescription
Registration Country : Denmark
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Desferal
Dosage Form : Injection/Infusion Solution
Dosage Strength : 500mg
Packaging :
Approval Date : 28/01/2015
Application Number : 20140606000012
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info :
Registration Country : Italy
Brand Name : DESFERAL
Dosage Form : Powder And Solvent For Injection
Dosage Strength : 500 mg/5 ml
Packaging : 10 UNITS 500 MG - PARENTERAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Withdrawn
Registration Country : Malta
Brand Name : Desferal
Dosage Form : Powder For Solution For Injection
Dosage Strength : 500MG
Packaging :
Approval Date : 2005-08-01
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Desferal
Dosage Form : Injection/Infusion Solution
Dosage Strength : 500mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway
Regulatory Info : Prescription
Registration Country : Denmark
Brand Name : Desferal
Dosage Form : Injection/Infusion Solution
Dosage Strength : 500mg
Packaging :
Approval Date : 12-11-1963
Application Number : 28100437363
Regulatory Info : Prescription
Registration Country : Denmark
Regulatory Info :
Registration Country : Italy
Brand Name : DEFEROXAMINA NORIDEM
Dosage Form : Powder For Solution For Injection
Dosage Strength : 500 mg
Packaging : 10 UNITS 500 MG - PARENTERAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Withdrawn
Registration Country : Malta
Brand Name : Desferrioxamine Mesilate
Dosage Form : Powder For Solution For Injection And Infusion
Dosage Strength : 500MG
Packaging :
Approval Date : 2010-01-29
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : Invalid
Registration Country : Malta
Brand Name : Desferal Vials,
Dosage Form : Solution For Injection
Dosage Strength : 500MG
Packaging :
Approval Date : 2019-08-27
Application Number :
Regulatory Info : Invalid
Registration Country : Malta
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
