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    Alprostadil

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    01 1Ethypharm

    02 7ENDO OPERATIONS

    03 1Ferring Pharmaceuticals

    04 1Flagship Biotech International Pvt. Ltd

    05 1Hikma Pharmaceuticals

    06 2Lifespan Biotech

    07 6Meda - Asker

    08 4Meda AB

    09 1Meitheal Pharmaceuticals

    10 1ORIFARM GROUP AS

    11 2Pfizer Consumer Healthcare

    12 38Pfizer Inc

    13 2Recordati

    14 4Sandoz B2B

    15 4Viatris

    16 2Xian Libang Pharmaceutical Co.,Ltd

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    Ethypharm

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    Virtual BoothEthypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.

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    Registration Country : France

    Alprostadil

    Brand Name :

    Dosage Form : Powder for Solution for Infusion

    Dosage Strength : 20MCG

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    Registration Country : France

    Ethypharm

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    02

    Pfizer Inc

    U.S.A
    euroPLX 86 Munich
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    Pfizer Inc

    U.S.A
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    Regulatory Info : RX

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    ALPROSTADIL

    Brand Name : PROSTIN VR PEDIATRIC

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.5MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18484

    Regulatory Info : RX

    Registration Country : USA

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    03

    Pfizer Inc

    U.S.A
    euroPLX 86 Munich
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    Pfizer Inc

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    Regulatory Info : RX

    Registration Country : USA

    ALPROSTADIL

    Brand Name : CAVERJECT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.01MG/VIAL

    Packaging :

    Approval Date : 1995-07-06

    Application Number : 20379

    Regulatory Info : RX

    Registration Country : USA

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    04

    Pfizer Inc

    U.S.A
    euroPLX 86 Munich
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    Pfizer Inc

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    ALPROSTADIL

    Brand Name : CAVERJECT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.02MG/VIAL

    Packaging :

    Approval Date : 1995-07-06

    Application Number : 20379

    Regulatory Info : RX

    Registration Country : USA

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    05

    Pfizer Inc

    U.S.A
    euroPLX 86 Munich
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    Pfizer Inc

    U.S.A
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    euroPLX 86 Munich
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : DISCN

    Registration Country : USA

    ALPROSTADIL

    Brand Name : CAVERJECT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.005MG/VIAL

    Packaging :

    Approval Date : 1996-06-27

    Application Number : 20379

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Pfizer Inc

    U.S.A
    euroPLX 86 Munich
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    Pfizer Inc

    U.S.A
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    euroPLX 86 Munich
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    ALPROSTADIL

    Brand Name : CAVERJECT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.04MG/VIAL

    Packaging :

    Approval Date : 1997-05-19

    Application Number : 20379

    Regulatory Info : RX

    Registration Country : USA

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    07

    Pfizer Inc

    U.S.A
    euroPLX 86 Munich
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    Pfizer Inc

    U.S.A
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    euroPLX 86 Munich
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    Regulatory Info : DISCN

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    ALPROSTADIL

    Brand Name : CAVERJECT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.005MG/ML

    Packaging :

    Approval Date : 1997-10-31

    Application Number : 20755

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Pfizer Inc

    U.S.A
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    Pfizer Inc

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    Regulatory Info : DISCN

    Registration Country : USA

    ALPROSTADIL

    Brand Name : CAVERJECT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.01MG/ML

    Packaging :

    Approval Date : 1997-10-01

    Application Number : 20755

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Pfizer Inc

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    Pfizer Inc

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    ALPROSTADIL

    Brand Name : CAVERJECT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.02MG/ML

    Packaging :

    Approval Date : 1997-10-01

    Application Number : 20755

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Viatris

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    Viatris

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    ALPROSTADIL

    Brand Name : MUSE

    Dosage Form : SUPPOSITORY;URETHRAL

    Dosage Strength : 0.125MG

    Packaging :

    Approval Date : 1996-11-19

    Application Number : 20700

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Viatris

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    Viatris

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : DISCN

    Registration Country : USA

    ALPROSTADIL

    Brand Name : MUSE

    Dosage Form : SUPPOSITORY;URETHRAL

    Dosage Strength : 0.25MG

    Packaging :

    Approval Date : 1996-11-19

    Application Number : 20700

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Viatris

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    Viatris

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    ALPROSTADIL

    Brand Name : MUSE

    Dosage Form : SUPPOSITORY;URETHRAL

    Dosage Strength : 0.5MG

    Packaging :

    Approval Date : 1996-11-19

    Application Number : 20700

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Viatris

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    Viatris

    U.S.A
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    euroPLX 86 Munich
    Not Confirmed
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : DISCN

    Registration Country : USA

    ALPROSTADIL

    Brand Name : MUSE

    Dosage Form : SUPPOSITORY;URETHRAL

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 1996-11-19

    Application Number : 20700

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    ENDO OPERATIONS

    Country
    euroPLX 86 Munich
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    euroPLX 86 Munich
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    Regulatory Info : DISCN

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    ALPROSTADIL

    Brand Name : EDEX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.005MG/VIAL

    Packaging :

    Approval Date : 1997-06-12

    Application Number : 20649

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    ENDO OPERATIONS

    Country
    euroPLX 86 Munich
    Not Confirmed
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    ENDO OPERATIONS

    Country
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    euroPLX 86 Munich
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    Brand Name : EDEX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.01MG/VIAL

    Packaging :

    Approval Date : 1997-06-12

    Application Number : 20649

    Regulatory Info : RX

    Registration Country : USA

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    16

    ENDO OPERATIONS

    Country
    euroPLX 86 Munich
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    ENDO OPERATIONS

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    euroPLX 86 Munich
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    Brand Name : EDEX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.02MG/VIAL

    Packaging :

    Approval Date : 1997-06-12

    Application Number : 20649

    Regulatory Info : RX

    Registration Country : USA

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    17

    ENDO OPERATIONS

    Country
    euroPLX 86 Munich
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    ENDO OPERATIONS

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    euroPLX 86 Munich
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    Brand Name : EDEX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.04MG/VIAL

    Packaging :

    Approval Date : 1997-06-12

    Application Number : 20649

    Regulatory Info : RX

    Registration Country : USA

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    18

    ENDO OPERATIONS

    Country
    euroPLX 86 Munich
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    ENDO OPERATIONS

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    euroPLX 86 Munich
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    ALPROSTADIL

    Brand Name : EDEX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.01MG/VIAL

    Packaging :

    Approval Date : 1998-07-30

    Application Number : 20649

    Regulatory Info : RX

    Registration Country : USA

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    19

    ENDO OPERATIONS

    Country
    euroPLX 86 Munich
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    ENDO OPERATIONS

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    euroPLX 86 Munich
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    Regulatory Info : RX

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    ALPROSTADIL

    Brand Name : EDEX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.02MG/VIAL

    Packaging :

    Approval Date : 1998-07-30

    Application Number : 20649

    Regulatory Info : RX

    Registration Country : USA

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    20

    ENDO OPERATIONS

    Country
    euroPLX 86 Munich
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    ENDO OPERATIONS

    Country
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    euroPLX 86 Munich
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    Regulatory Info : RX

    Registration Country : USA

    ALPROSTADIL

    Brand Name : EDEX

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 0.04MG/VIAL

    Packaging :

    Approval Date : 1998-07-30

    Application Number : 20649

    Regulatory Info : RX

    Registration Country : USA

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