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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Abon Pharmaceuticals

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    01 1ATOVAQUONE

    02 1CLOFARABINE

    03 1GABAPENTIN

    04 1SUCRALFATE

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    01

    Brand Name : ATOVAQUONE

    U.S.A
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    Brand Name : ATOVAQUONE

    U.S.A
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    RLD : No

    TE Code : AB

    ATOVAQUONE

    Abon Pharmaceuticals

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : ATOVAQUONE

    Dosage Strength : 750MG/5ML

    Approval Date : 2021-10-25

    Application Number : 214272

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    02

    Brand Name : CLOFARABINE

    U.S.A
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    Brand Name : CLOFARABINE

    U.S.A
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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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    03

    Brand Name : GABAPENTIN

    U.S.A
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    Brand Name : GABAPENTIN

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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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    04

    Brand Name : SUCRALFATE

    U.S.A
    BioAsia
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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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