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

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    Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

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

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    FAMAR CDMO- From early development to commercial manufacturing.

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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    Abon Pharmaceuticals

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    FINISHED DOSAGE FORMULATIONS

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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
    CAMX
    Not Confirmed
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    Brand Name : CLOFARABINE

    U.S.A
    CAMX
    Not Confirmed
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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
    CAMX
    Not Confirmed
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    Brand Name : GABAPENTIN

    U.S.A
    CAMX
    Not Confirmed
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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
    CAMX
    Not Confirmed
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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
    CAMX
    Not Confirmed
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    Brand Name : VANCOMYCIN HYDROCHLO...

    U.S.A
    CAMX
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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
    CAMX
    Not Confirmed
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    Brand Name : VANCOMYCIN HYDROCHLO...

    U.S.A
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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
    CAMX
    Not Confirmed
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    Brand Name : VENLAFAXINE HYDROCHL...

    U.S.A
    CAMX
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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
    CAMX
    Not Confirmed
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    Brand Name : VENLAFAXINE HYDROCHL...

    U.S.A
    CAMX
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    • fda
    • EDQM
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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 : 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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