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

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    xyz-pharma-m-2025-03-24

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

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    Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.

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    xyz-pharma-m-2025-03-17

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    Abon Pharmaceuticals

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    FINISHED DOSAGE FORMULATIONS

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    01 1ATOVAQUONE

    02 1CLOFARABINE

    03 1GABAPENTIN

    04 1SUCRALFATE

    05 2VENLAFAXINE HYDROCHLORIDE

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    01

    Brand Name : ATOVAQUONE

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    Brand Name : ATOVAQUONE

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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

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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
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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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    05

    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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    06

    Brand Name : VENLAFAXINE HYDROCHL...

    U.S.A
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    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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