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    Approved Drug Products containing Alqoverin listed in the FDA Orange Book. Original Data : FDA Website

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    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    xyz-pharma-m-2024-09-09

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    xyz-pharma-m-2024-09-09

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    Alqoverin

    ACTIVE PHARMA INGREDIENTS

    PRICE INFORMATION

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    DIGITAL CONTENT

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    $ API Ref.Price (USD/KG) : 36Xls

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    01 2SANOFI AVENTIS US

    02 1CHARTWELL RX

    03 1FOSUN PHARMA

    04 1IVAX PHARMS

    05 2NOVARTIS

    06 2SUN PHARM INDUSTRIES

    07 3WATSON LABS

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    01

    SANOFI AVENTIS US

    France
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    CPhI Worldwide, Milan
    Attending
    • fda
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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 :

    PHENYLBUTAZONE

    Brand Name : AZOLID

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 87091

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    SANOFI AVENTIS US

    France
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    CPhI Worldwide, Milan
    Attending
    • fda
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    • WHO-GMP

    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 :

    PHENYLBUTAZONE

    Brand Name : AZOLID

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 87260

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    Sanofi Company Banner

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    03

    WATSON LABS

    Ireland
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    WATSON LABS

    Ireland
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    RLD : No

    TE Code :

    PHENYLBUTAZONE

    Brand Name : PHENYLBUTAZONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 86151

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    WATSON LABS

    Ireland
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    WATSON LABS

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    RLD : No

    TE Code :

    PHENYLBUTAZONE

    Brand Name : PHENYLBUTAZONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-04-21

    Application Number : 87674

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    05

    WATSON LABS

    Ireland
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    WATSON LABS

    Ireland
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    Formnext Forum
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    RLD : No

    TE Code :

    PHENYLBUTAZONE

    Brand Name : PHENYLBUTAZONE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-12-17

    Application Number : 87756

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    CHARTWELL RX

    U.S.A
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    CHARTWELL RX

    U.S.A
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    RLD : No

    TE Code :

    PHENYLBUTAZONE

    Brand Name : PHENYLBUTAZONE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-06-16

    Application Number : 87774

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    FOSUN PHARMA

    China
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    FOSUN PHARMA

    China
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    RLD : No

    TE Code :

    PHENYLBUTAZONE

    Brand Name : PHENYLBUTAZONE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 84339

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    IVAX PHARMS

    U.S.A
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    IVAX PHARMS

    U.S.A
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    RLD : No

    TE Code :

    PHENYLBUTAZONE

    Brand Name : PHENYLBUTAZONE

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1983-06-24

    Application Number : 88218

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    NOVARTIS

    Switzerland
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    NOVARTIS

    Switzerland
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    Formnext Forum
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    RLD : No

    TE Code :

    PHENYLBUTAZONE

    Brand Name : BUTAZOLIDIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 8319

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    10

    NOVARTIS

    Switzerland
    Formnext Forum
    Not Confirmed
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    NOVARTIS

    Switzerland
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    Formnext Forum
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    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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    Flag Switzerland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    PHENYLBUTAZONE

    Brand Name : BUTAZOLIDIN

    Dosage Form : CAPSULE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 8319

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

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    Website

    Corporate PDF