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    Approved Drug Products of Praxgen listed in the FDA Orange Book. Original Data : FDA Website

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

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    Bora Pharmaceuticals- Making success more certain.

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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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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    Praxgen

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    FINISHED DOSAGE FORMULATIONS

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    01 1DOXYCYCLINE HYCLATE

    02 1LEVOLEUCOVORIN CALCIUM

    03 1METHYLPREDNISOLONE

    04 2RANOLAZINE

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    01

    Brand Name : DOXYCYCLINE HYCLATE

    U.S.A
    FNCE 2024
    Not Confirmed
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    Brand Name : DOXYCYCLINE HYCLATE

    U.S.A
    FNCE 2024
    Not Confirmed
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    • WHO-GMP
    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 :

    DOXYCYCLINE HYCLATE

    Praxgen

    Dosage Form : TABLET; ORAL

    Proprietary Name : DOXYCYCLINE HYCLATE

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2022-03-30

    Application Number : 212487

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : LEVOLEUCOVORIN CALCI...

    U.S.A
    FNCE 2024
    Not Confirmed
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    Brand Name : LEVOLEUCOVORIN CALCI...

    U.S.A
    FNCE 2024
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    LEVOLEUCOVORIN CALCIUM

    Praxgen

    Dosage Form : SOLUTION; INTRAVENOUS

    Proprietary Name : LEVOLEUCOVORIN CALCIUM

    Dosage Strength : EQ 175MG BASE/17.5ML (EQ...

    Approval Date : 2021-11-02

    Application Number : 213797

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    Brand Name : METHYLPREDNISOLONE

    U.S.A
    FNCE 2024
    Not Confirmed
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    Brand Name : METHYLPREDNISOLONE

    U.S.A
    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    METHYLPREDNISOLONE

    Praxgen

    Dosage Form : TABLET; ORAL

    Proprietary Name : METHYLPREDNISOLONE

    Dosage Strength : 4MG

    Approval Date : 2019-06-27

    Application Number : 212262

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    Brand Name : RANOLAZINE

    U.S.A
    FNCE 2024
    Not Confirmed
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    Brand Name : RANOLAZINE

    U.S.A
    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code : AB

    RANOLAZINE

    Praxgen

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : RANOLAZINE

    Dosage Strength : 500MG

    Approval Date : 2020-03-23

    Application Number : 212781

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : RANOLAZINE

    U.S.A
    FNCE 2024
    Not Confirmed
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    Brand Name : RANOLAZINE

    U.S.A
    FNCE 2024
    Not Confirmed
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    • fda
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    RLD : No

    TE Code : AB

    RANOLAZINE

    Praxgen

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : RANOLAZINE

    Dosage Strength : 1GM

    Approval Date : 2020-03-23

    Application Number : 212781

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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