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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

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

DAUNORUBICIN HYDROCHLORIDE

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

Sanofi Company Banner

02

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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

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03

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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

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04

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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

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05

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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

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06

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

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

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07

ASPEN
Not Confirmed
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Daunorubicin Hydrochloride

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

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08

ASPEN
Not Confirmed
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Not Confirmed

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

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09

ASPEN
Not Confirmed
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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

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10

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

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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11

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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

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12

ASPEN
Not Confirmed
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ASPEN
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Daunorubicin HCl

Brand Name :

Dosage Form : Lyophilised Inj.

Dosage Strength : 20MG/Vial

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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13

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Daunorubicin Hydrochloride

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

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14

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Daunorubicin Hydrochloride

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

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15

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

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

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16

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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

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17

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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

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18

ASPEN
Not Confirmed
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DAUNORUBICIN HYDROCHLORIDE

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

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19

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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

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20

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

DAUNORUBICIN HYDROCHLORIDE

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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