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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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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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    Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.

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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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    Fishfa Biogenics: Renowned Manufacturer, & Exporter of Tacrolimus & Mupirocin API.

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    Abon Pharmaceuticals

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    01 1CLOFARABINE

    02 2ERYTHROMYCIN

    03 1GABAPENTIN

    04 1SUCRALFATE

    05 2VANCOMYCIN HYDROCHLORIDE

    06 2VENLAFAXINE HYDROCHLORIDE

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    01

    Brand Name : CLOFARABINE

    U.S.A
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    Brand Name : CLOFARABINE

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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 : ERYTHROMYCIN

    U.S.A
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    Brand Name : ERYTHROMYCIN

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    RLD : No

    TE Code : AB

    ERYTHROMYCIN

    Abon Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : ERYTHROMYCIN

    Dosage Strength : 250MG

    Approval Date : 2025-09-23

    Application Number : 219691

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    Brand Name : ERYTHROMYCIN

    U.S.A
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    Brand Name : ERYTHROMYCIN

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    RLD : No

    TE Code : AB

    ERYTHROMYCIN

    Abon Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : ERYTHROMYCIN

    Dosage Strength : 500MG

    Approval Date : 2025-09-23

    Application Number : 219691

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    04

    Brand Name : GABAPENTIN

    U.S.A
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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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    05

    Brand Name : SUCRALFATE

    U.S.A
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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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    06

    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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    07

    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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    08

    Brand Name : VENLAFAXINE HYDROCHL...

    U.S.A
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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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    09

    Brand Name : VENLAFAXINE HYDROCHL...

    U.S.A
    Neuroscience
    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 225MG BASE

    Approval Date : 2025-02-07

    Application Number : 217841

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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