Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 2Sanofi
02 1Naprod Life Sciences
03 2Fresenius Kabi USA
04 3Hikma Pharmaceuticals
05 1Meitheal Pharmaceuticals
06 1ORIFARM GROUP AS
07 1SEARCHLIGHT PHARMA
08 2Teva Pharmaceutical Industries
09 1Wyeth Pharmaceuticals Inc
10 2Zhejiang Hisun Pharmaceutical
01 11INJECTABLE;INJECTION
02 1Lyophilised Inj.
03 1POWDER FOR SOLUTION
04 2POWDER FOR SOLUTION FOR INFUSION
05 1SOLUTION
01 5DISCN
02 2Prescription
03 6RX
04 3Blank
01 4CERUBIDINE
02 1Cerubidin
03 1Cerubidine
04 8DAUNORUBICIN HYDROCHLORIDE
05 1DAUNORUBICIN HYDROCHLORIDE INJECTION
06 1Blank
01 2Canada
02 1India
03 2Sweden
04 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
Naprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.
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
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info :
Registration Country : Sweden
Brand Name : Cerubidin
Dosage Form : POWDER FOR SOLUTION FOR INFUSION
Dosage Strength : 20 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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 : 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 : Sweden
Brand Name : Cerubidine
Dosage Form : POWDER FOR SOLUTION FOR INFUSION
Dosage Strength : 20 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
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
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