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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Daunorubicin HCl

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    01 1SANOFI AVENTIS US

    02 2FRESENIUS KABI USA

    03 2HIKMA

    04 2HISUN PHARM HANGZHOU

    05 1MEITHEAL

    06 2TEVA PARENTERAL

    07 1WYETH AYERST

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    01

    SANOFI AVENTIS US

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

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    RLD : No

    TE Code :

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : CERUBIDINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/VIAL

    Approval Date : 1982-01-01

    Application Number : 61876

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    FRESENIUS KABI USA

    U.S.A
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    FRESENIUS KABI USA

    U.S.A
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    RLD : No

    TE Code : AP

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : DAUNORUBICIN HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/VIAL

    Approval Date : 1999-05-25

    Application Number : 65000

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    03

    FRESENIUS KABI USA

    U.S.A
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    FRESENIUS KABI USA

    U.S.A
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    RLD : No

    TE Code :

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : DAUNORUBICIN HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/VIAL

    Approval Date : 2001-11-20

    Application Number : 65034

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    04

    HIKMA

    United Kingdom
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    RLD : Yes

    TE Code : AP

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : DAUNORUBICIN HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Approval Date : 1998-01-30

    Application Number : 50731

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AP

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    05

    HIKMA

    United Kingdom
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    HIKMA

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    RLD : No

    TE Code : AP

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : CERUBIDINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/VIAL

    Approval Date : 1995-02-03

    Application Number : 64103

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    06

    MEITHEAL

    U.S.A
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    MEITHEAL

    U.S.A
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    RLD : No

    TE Code : AP

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : DAUNORUBICIN HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Approval Date : 2000-01-24

    Application Number : 65035

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    07

    TEVA PARENTERAL

    Israel
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    TEVA PARENTERAL

    Israel
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    RLD : No

    TE Code :

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : DAUNORUBICIN HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/VIAL

    Approval Date : 1998-06-23

    Application Number : 64212

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    TEVA PARENTERAL

    Israel
    Antibody Engineering
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    TEVA PARENTERAL

    Israel
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    Antibody Engineering
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    RLD : No

    TE Code :

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : DAUNORUBICIN HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 50MG BASE/VIAL

    Approval Date : 1999-05-03

    Application Number : 64212

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    WYETH AYERST

    U.S.A
    Antibody Engineering
    Not Confirmed
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    WYETH AYERST

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    RLD : No

    TE Code :

    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**

    Approval Date : 1982-01-01

    Application Number : 50484

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    HISUN PHARM HANGZHOU

    China
    Antibody Engineering
    Not Confirmed
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    HISUN PHARM HANGZHOU

    China
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    Antibody Engineering
    Not Confirmed
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    RLD : No

    TE Code :

    DAUNORUBICIN HYDROCHLORIDE

    Brand Name : DAUNORUBICIN HYDROCHLORIDE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG BASE/VIAL

    Approval Date : 2019-04-25

    Application Number : 206195

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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