Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 2Fresenius Kabi USA
03 4Hikma Pharmaceuticals
04 3Jazz Pharmaceuticals
05 1Meitheal Pharmaceuticals
06 1Naprod Life Sciences
07 1ORIFARM GROUP AS
08 1Pfizer Inc
09 1SEARCHLIGHT PHARMA
10 2Teva Pharmaceutical Industries
11 1Wyeth Pharmaceuticals Inc
12 2Zhejiang Hisun Pharmaceutical
01 11INJECTABLE;INJECTION
02 1Infusion Solution
03 1Lyophilised Inj.
04 1POWDER FOR SOLUTION
05 1Powder And Solvent For Injectable Solution
06 1Powder For Concentrate For Infusion Solution
07 2Powder For Concentrate For Solution For Infusion
08 1SOLUTION
09 1Solution For Injection
01 1Approved
02 2Authorized
03 6DISCN
04 5Prescription
05 5RX
06 1Blank
01 4CERUBIDINE
02 1Cerubidine
03 8DAUNORUBICIN HYDROCHLORIDE
04 1DAUNORUBICIN HYDROCHLORIDE INJECTION
05 1Daunoblastin
06 1Daunorubicin "Hikma"
07 3Vyxeos Liposomal
08 1Blank
01 2Canada
02 3Denmark
03 1India
04 2Spain
05 1Sweden
06 11USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CERUBIDINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 61876
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DAUNORUBICIN HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/VIAL
Packaging :
Approval Date : 1999-05-25
Application Number : 65000
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DAUNORUBICIN HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/VIAL
Packaging :
Approval Date : 2001-11-20
Application Number : 65034
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DAUNORUBICIN HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML
Packaging :
Approval Date : 1998-01-30
Application Number : 50731
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CERUBIDINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/VIAL
Packaging :
Approval Date : 1995-02-03
Application Number : 64103
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Prescription
Registration Country : Canada
DAUNORUBICIN (DAUNORUBICIN HYDROCHLORIDE)
Brand Name : DAUNORUBICIN HYDROCHLORIDE INJECTION
Dosage Form : SOLUTION
Dosage Strength : 20MG/4ML
Packaging :
Approval Date :
Application Number : 2539209
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Denmark
Brand Name : Daunorubicin \"Hikma\"
Dosage Form : Infusion Solution
Dosage Strength : 5mg/ml
Packaging :
Approval Date : 21-08-2025
Application Number : 28106903323
Regulatory Info : Prescription
Registration Country : Denmark
Regulatory Info : Authorized
Registration Country : Spain
Cytharabine; Daunorubicin Hydrochloride
Brand Name : Vyxeos Liposomal
Dosage Form : Powder For Concentrate For Infusion Solution
Dosage Strength : 44MG; 100 MG
Packaging :
Approval Date : 19-12-2018
Application Number : 1181308001
Regulatory Info : Authorized
Registration Country : Spain
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
Regulatory Info : Approved
Registration Country : Sweden
Cytarabine; Daunorubicin Hydrochloride
Brand Name : Vyxeos Liposomal
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 44mg/100mg
Packaging :
Approval Date : 23-08-2018
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : RX
Registration Country : USA
Brand Name : DAUNORUBICIN HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML
Packaging :
Approval Date : 2000-01-24
Application Number : 65035
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Lyophilised Inj.
Dosage Strength : 20MG/Vial
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : Prescription
Registration Country : Denmark
Brand Name : Cerubidine
Dosage Form : Solution For Injection
Dosage Strength : 20mg
Packaging :
Approval Date : 09-08-1995
Application Number : 28101699994
Regulatory Info : Prescription
Registration Country : Denmark
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Daunoblastin
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 20MG
Packaging :
Approval Date : 01-11-1968
Application Number : 46427
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Prescription
Registration Country : Canada
DAUNORUBICIN (DAUNORUBICIN HYDROCHLORIDE)
Brand Name : CERUBIDINE
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date :
Application Number : 1926683
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DAUNORUBICIN HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/VIAL
Packaging :
Approval Date : 1998-06-23
Application Number : 64212
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DAUNORUBICIN HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 50MG BASE/VIAL
Packaging :
Approval Date : 1999-05-03
Application Number : 64212
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CERUBIDINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 50484
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DAUNORUBICIN HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 20MG BASE/VIAL
Packaging :
Approval Date : 2019-04-25
Application Number : 206195
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DAUNORUBICIN HYDROCHLORIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 5MG BASE/ML
Packaging :
Approval Date : 2019-04-12
Application Number : 208759
Regulatory Info : RX
Registration Country : USA
