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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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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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    TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Abon Pharmaceuticals

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    01 1CLOFARABINE

    02 1GABAPENTIN

    03 1SUCRALFATE

    04 2VANCOMYCIN HYDROCHLORIDE

    05 2VENLAFAXINE HYDROCHLORIDE

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    01

    Brand Name : CLOFARABINE

    U.S.A
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    Brand Name : CLOFARABINE

    U.S.A
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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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    RLD : No

    TE Code :

    CLOFARABINE

    Abon Pharmaceuticals

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : CLOFARABINE

    Dosage Strength : 20MG/20ML (1MG/ML)

    Approval Date : 2017-05-09

    Application Number : 204029

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : GABAPENTIN

    U.S.A
    ISPE Annual Meeting
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    Brand Name : GABAPENTIN

    U.S.A
    ISPE Annual Meeting
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    RLD : No

    TE Code : AB2

    GABAPENTIN

    Abon Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : GABAPENTIN

    Dosage Strength : 600MG

    Approval Date : 2024-09-09

    Application Number : 203643

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB2

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    03

    Brand Name : SUCRALFATE

    U.S.A
    ISPE Annual Meeting
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    Brand Name : SUCRALFATE

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    RLD : No

    TE Code : AB

    SUCRALFATE

    Abon Pharmaceuticals

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : SUCRALFATE

    Dosage Strength : 1GM/10ML

    Approval Date : 2024-03-21

    Application Number : 216726

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : VANCOMYCIN HYDROCHLO...

    U.S.A
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    Brand Name : VANCOMYCIN HYDROCHLO...

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    RLD : No

    TE Code :

    VANCOMYCIN HYDROCHLORIDE

    Abon Pharmaceuticals

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : VANCOMYCIN HYDROCHLORIDE

    Dosage Strength : EQ 125MG BASE

    Approval Date : 2012-04-09

    Application Number : 65478

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : VANCOMYCIN HYDROCHLO...

    U.S.A
    ISPE Annual Meeting
    Not Confirmed
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    Brand Name : VANCOMYCIN HYDROCHLO...

    U.S.A
    ISPE Annual Meeting
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    RLD : No

    TE Code :

    VANCOMYCIN HYDROCHLORIDE

    Abon Pharmaceuticals

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : VANCOMYCIN HYDROCHLORIDE

    Dosage Strength : EQ 250MG BASE

    Approval Date : 2012-04-09

    Application Number : 65478

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    Brand Name : VENLAFAXINE HYDROCHL...

    U.S.A
    ISPE Annual Meeting
    Not Confirmed
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    Brand Name : VENLAFAXINE HYDROCHL...

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    RLD : No

    TE Code : AB

    VENLAFAXINE HYDROCHLORIDE

    Abon Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : VENLAFAXINE HYDROCHLORID...

    Dosage Strength : EQ 150MG BASE

    Approval Date : 2025-02-07

    Application Number : 217841

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : VENLAFAXINE HYDROCHL...

    U.S.A
    ISPE Annual Meeting
    Not Confirmed
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    Brand Name : VENLAFAXINE HYDROCHL...

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    ISPE Annual Meeting
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    RLD : No

    TE Code : AB

    VENLAFAXINE HYDROCHLORIDE

    Abon Pharmaceuticals

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : VENLAFAXINE HYDROCHLORID...

    Dosage Strength : EQ 225MG BASE

    Approval Date : 2025-02-07

    Application Number : 217841

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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