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    Us Worldmeds's list of EU CTD Dossiers, Marketing Authorizations, In, Out Licensing Opportunities & Finished Dosage Formulations aggregated by PharmaCompass

    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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    FINISHED DOSAGE FORMULATIONS

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    01 1DANTROLENE SODIUM

    02 1EFLORNITHINE HYDROCHLORIDE

    03 1LOFEXIDINE HYDROCHLORIDE

    04 1MELPHALAN HYDROCHLORIDE

    05 5NADOLOL

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    01

    Brand Name : REVONTO

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : REVONTO

    U.S.A
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    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    DANTROLENE SODIUM

    US WorldMeds

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : REVONTO

    Dosage Strength : 20MG/VIAL

    Packaging :

    Approval Date : 2007-07-24

    Application Number : 78378

    Regulatory Info : RX

    Registration Country : USA

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    02

    Brand Name : IWILFIN

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : IWILFIN

    U.S.A
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    Discovery on Target
    Not Confirmed
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    • EDQM
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    Regulatory Info : RX

    Registration Country : USA

    EFLORNITHINE HYDROCHLORIDE

    US WorldMeds

    Dosage Form : TABLET;ORAL

    Brand Name : IWILFIN

    Dosage Strength : EQ 192MG BASE

    Packaging :

    Approval Date : 2023-12-13

    Application Number : 215500

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : LUCEMYRA

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : LUCEMYRA

    U.S.A
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    Discovery on Target
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    Regulatory Info : RX

    Registration Country : USA

    LOFEXIDINE HYDROCHLORIDE

    US WorldMeds

    Dosage Form : TABLET;ORAL

    Brand Name : LUCEMYRA

    Dosage Strength : EQ 0.18MG BASE

    Packaging :

    Approval Date : 2018-05-16

    Application Number : 209229

    Regulatory Info : RX

    Registration Country : USA

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    04

    Brand Name : MELPHALAN HYDROCHLOR...

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : MELPHALAN HYDROCHLOR...

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    MELPHALAN HYDROCHLORIDE

    US WorldMeds

    Dosage Form : INJECTABLE;INJECTION

    Brand Name : MELPHALAN HYDROCHLORIDE

    Dosage Strength : EQ 50MG BASE/VIAL

    Packaging :

    Approval Date : 2019-05-03

    Application Number : 207032

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Brand Name : CORGARD

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : CORGARD

    U.S.A
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    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET;ORAL

    Brand Name : CORGARD

    Dosage Strength : 40MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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    Market
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    06

    Brand Name : CORGARD

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : CORGARD

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET;ORAL

    Brand Name : CORGARD

    Dosage Strength : 80MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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    Market
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    07

    Brand Name : CORGARD

    U.S.A
    Discovery on Target
    Not Confirmed
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    Brand Name : CORGARD

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET;ORAL

    Brand Name : CORGARD

    Dosage Strength : 120MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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    Market
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    08

    Brand Name : CORGARD

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Brand Name : CORGARD

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • 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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    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET;ORAL

    Brand Name : CORGARD

    Dosage Strength : 160MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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    Product
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    Market
    Place

    09

    Brand Name : CORGARD

    U.S.A
    Discovery on Target
    Not Confirmed
    arrow

    Brand Name : CORGARD

    U.S.A
    arrow
    Discovery on Target
    Not Confirmed
    • fda
    • EDQM
    • 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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    Flag U.S.A
    Virtual Booth Virtual Booth
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    Regulatory Info : DISCN

    Registration Country : USA

    NADOLOL

    US WorldMeds

    Dosage Form : TABLET;ORAL

    Brand Name : CORGARD

    Dosage Strength : 20MG

    Packaging :

    Approval Date : 1986-10-28

    Application Number : 18063

    Regulatory Info : DISCN

    Registration Country : USA

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