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    Bleomycin Sulphate

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

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    01 2BRISTOL MYERS SQUIBB

    02 1CIPLA

    03 2FRESENIUS KABI USA

    04 2HIKMA

    05 2HOSPIRA

    06 2MEITHEAL

    07 1PHARMACHEMIE BV

    08 2TEVA PARENTERAL

    09 2TEVA PHARMS USA

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    01

    BRISTOL MYERS SQUIBB

    U.S.A
    BioAsia
    Not Confirmed
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    BRISTOL MYERS SQUIBB

    U.S.A
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    BioAsia
    Not Confirmed
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    RLD : Yes

    TE Code :

    BLEOMYCIN SULFATE

    Brand Name : BLENOXANE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 15 UNITS BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 50443

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    02

    BRISTOL MYERS SQUIBB

    U.S.A
    BioAsia
    Not Confirmed
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    BRISTOL MYERS SQUIBB

    U.S.A
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    RLD : Yes

    TE Code :

    BLEOMYCIN SULFATE

    Brand Name : BLENOXANE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 30 UNITS BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1995-09-07

    Application Number : 50443

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    03

    HIKMA

    United Kingdom
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    RLD : No

    TE Code : AP

    BLEOMYCIN SULFATE

    Brand Name : BLEOMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 30 UNITS BASE/VIAL

    Approval Date : 2001-10-17

    Application Number : 65042

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    04

    HIKMA

    United Kingdom
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    RLD : No

    TE Code : AP

    BLEOMYCIN SULFATE

    Brand Name : BLEOMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 15 UNITS BASE/VIAL

    Approval Date : 2001-10-17

    Application Number : 65042

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    05

    HOSPIRA

    U.S.A
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    U.S.A
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    RLD : No

    TE Code : AP

    BLEOMYCIN SULFATE

    Brand Name : BLEOMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 15 UNITS BASE/VIAL

    Approval Date : 2000-03-10

    Application Number : 65031

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    06

    HOSPIRA

    U.S.A
    BioAsia
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    U.S.A
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    RLD : No

    TE Code : AP

    BLEOMYCIN SULFATE

    Brand Name : BLEOMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 30 UNITS BASE/VIAL

    Approval Date : 2000-03-10

    Application Number : 65031

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    07

    TEVA PARENTERAL

    Israel
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    TEVA PARENTERAL

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    RLD : No

    TE Code :

    BLEOMYCIN SULFATE

    Brand Name : BLEOMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 15 UNITS BASE/VIAL

    Approval Date : 1996-06-01

    Application Number : 64084

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    TEVA PARENTERAL

    Israel
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    RLD : No

    TE Code :

    BLEOMYCIN SULFATE

    Brand Name : BLEOMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 30 UNITS BASE/VIAL

    Approval Date : 1996-06-01

    Application Number : 64084

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    TEVA PHARMS USA

    Israel
    BioAsia
    Not Confirmed
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    TEVA PHARMS USA

    Israel
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    BioAsia
    Not Confirmed
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    RLD : No

    TE Code :

    BLEOMYCIN SULFATE

    Brand Name : BLEOMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 15 UNITS BASE/VIAL

    Approval Date : 2000-06-27

    Application Number : 65033

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    TEVA PHARMS USA

    Israel
    BioAsia
    Not Confirmed
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    TEVA PHARMS USA

    Israel
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    BioAsia
    Not Confirmed
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    RLD : No

    TE Code :

    BLEOMYCIN SULFATE

    Brand Name : BLEOMYCIN SULFATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 30 UNITS BASE/VIAL

    Approval Date : 2000-06-27

    Application Number : 65033

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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