Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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01 1Sanofi
02 1Accure Labs
03 1Aprazer
04 1Diatos Sa
05 1Hikma Pharmaceuticals
06 1JV Healthcare Limited
07 10Jazz Pharmaceuticals
08 1ORIFARM GROUP AS
09 4Pfizer Inc
10 1Sakar Healthcare
11 1TherDose Pharma
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01 1Concentrate For Solution For Infusion
02 1Daunorubicin 20Mg 10Ml 1 Units Parenteral Use
03 1Dispersion For Infusion
04 1INJECTION
05 1Infusion Solution
06 3Injection
07 1POI
08 1POWDER
09 1POWDER;INTRAVENOUS
10 1Powder And Solvent For Injection Solution
11 4Powder For Concentrate For Solution For Infusion
12 3Solution For Injection
13 4Blank
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01 2Allowed
02 3Approved
03 1Authorised
04 1Deregistered
05 1Generic
06 1Marketed
07 1Originator
08 4Prescription
09 1RX
10 8Blank
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01 3Cerubidine
02 1DAUNOTHER
03 1DAUNOZER
04 2Daunoblastin
05 2Daunoblastina
06 1Daunorubicin Hikma
07 1Daunoxome
08 2VYXEOS
09 4Vyxeos
10 2Vyxeos Liposomal
11 1Vyxeos liposomal
12 1Vyxeos liposomal mg
13 2Blank
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01 4Australia
02 1Canada
03 1Denmark
04 2Estonia
05 4India
06 1Italy
07 1Malta
08 1Norway
09 1South Africa
10 4Sweden
11 2Switzerland
12 1USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Cerubidine
Dosage Form : Solution For Injection
Dosage Strength : 20mg
Packaging :
Approval Date : 04-05-1977
Application Number : 1.98E+13
Regulatory Info : Approved
Registration Country : Sweden
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Regulatory Info : Generic
Registration Country : India
Brand Name :
Dosage Form : INJECTION
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : India

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Regulatory Info :
Registration Country : India
Brand Name : DAUNOZER
Dosage Form : Injection
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India

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Regulatory Info : RX
Registration Country : USA
Brand Name : VYXEOS
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 100MG;44MG
Packaging :
Approval Date : 2017-08-03
Application Number : 209401
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Vyxeos liposomal mg
Dosage Form : Dispersion For Infusion
Dosage Strength : 44mg;100mg
Packaging :
Approval Date : 17/02/2022
Application Number : 68014
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Vyxeos liposomal
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 44mg; 100mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Vyxeos Liposomal
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 100mg; 44mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Prescription
Registration Country : Canada
Brand Name : VYXEOS
Dosage Form : POWDER
Dosage Strength : 44MG
Packaging :
Approval Date :
Application Number : 2515490
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info :
Registration Country : Australia
Brand Name : Vyxeos
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia

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Regulatory Info :
Registration Country : Australia
Brand Name : Vyxeos
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia

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Regulatory Info :
Registration Country : Australia
Brand Name : Vyxeos
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia

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Regulatory Info :
Registration Country : Australia
Brand Name : Vyxeos
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia

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Regulatory Info : Prescription
Registration Country : Denmark
Cytarabin; Daunorubicin Hydrochloride
Brand Name : Vyxeos Liposomal
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 44mg; 100mg
Packaging :
Approval Date : 27-08-2018
Application Number : 28106031517
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info :
Registration Country : Italy
Brand Name : Daunoblastina
Dosage Form : Daunorubicin 20Mg 10Ml 1 Units Parenteral Use
Dosage Strength : 1 vial EV 20 mg + 1 ampoule solv 10 ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Daunoblastin
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 20mg
Packaging :
Approval Date : 04/11/2021
Application Number : 68340
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Prescription
Registration Country : Estonia
Brand Name : Daunoblastina
Dosage Form : Solution For Injection
Dosage Strength : 20mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Daunoblastin
Dosage Form : POI
Dosage Strength : 20mg
Packaging : 1X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa

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Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 20MG
Packaging : 10 ml + WFI
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India

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Regulatory Info :
Registration Country : India
Brand Name : DAUNOTHER
Dosage Form : Injection
Dosage Strength : 20mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India

Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Cerubidine
Dosage Form : Powder And Solvent For Injection Solution
Dosage Strength : 20MG
Packaging :
Approval Date : 2023-10-09
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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