Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 2Fresenius Kabi USA
03 3Hikma Pharmaceuticals
04 2Jazz Pharmaceuticals
05 1Meitheal Pharmaceuticals
06 1Naprod Life Sciences
07 1Pfizer Inc
08 1SEARCHLIGHT PHARMA
09 2Teva Pharmaceutical Industries
10 1Wyeth Pharmaceuticals Inc
11 2Zhejiang Hisun Pharmaceutical
01 11INJECTABLE;INJECTION
02 1Lyophilised Inj.
03 1POWDER FOR SOLUTION
04 1Powder And Solvent For Injectable Solution
05 1Powder For Concentrate For Infusion Solution
06 1Powder For Concentrate For Solution For Infusion
07 1SOLUTION
01 1Approved
02 2Authorized
03 5DISCN
04 2Prescription
05 6RX
06 1Blank
01 4CERUBIDINE
02 8DAUNORUBICIN HYDROCHLORIDE
03 1DAUNORUBICIN HYDROCHLORIDE INJECTION
04 1Daunoblastin
05 2Vyxeos Liposomal
06 1Blank
01 2Canada
02 1India
03 2Spain
04 1Sweden
05 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 : RX
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 : RX
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 : 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 : 20171103000069
Regulatory Info : Approved
Registration Country : Sweden
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 : 2018-12-19
Application Number : 1181308001
Regulatory Info : Authorized
Registration Country : Spain
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 : Authorized
Registration Country : Spain
Brand Name : Daunoblastin
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 20MG
Packaging :
Approval Date : 1968-11-01
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
