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

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    Munit offers scalable GMP micronization and particle size engineering to enhance drug solubility, bioavailability, and performance.

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    Mission CDMO team brings reliability, resourcefulness, & responsiveness in executing your development project.

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    Jai Radhe Sales is your partner for all your sourcing needs.

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    01 5APOMORPHINE HYDROCHLORIDE

    02 4ESLICARBAZEPINE ACETATE

    03 1ESTRADIOL; NORETHINDRONE ACETATE; RELUGOLIX

    04 1GLYCOPYRROLATE

    05 1RELUGOLIX

    06 1VIBEGRON

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    01

    Brand Name : KYNMOBI

    U.S.A
    Bio-Europe Autumn
    Not Confirmed
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    Brand Name : KYNMOBI

    U.S.A
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    Bio-Europe Autumn
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    Regulatory Info : DISCN

    Registration Country : USA

    APOMORPHINE HYDROCHLORIDE

    Sumitomo Pharma America

    Dosage Form : FILM;SUBLINGUAL

    Brand Name : KYNMOBI

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2020-05-21

    Application Number : 210875

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Brand Name : KYNMOBI

    U.S.A
    Bio-Europe Autumn
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    Brand Name : KYNMOBI

    U.S.A
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    Bio-Europe Autumn
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    Regulatory Info : DISCN

    Registration Country : USA

    APOMORPHINE HYDROCHLORIDE

    Sumitomo Pharma America

    Dosage Form : FILM;SUBLINGUAL

    Brand Name : KYNMOBI

    Dosage Strength : 15MG

    Packaging :

    Approval Date : 2020-05-21

    Application Number : 210875

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Brand Name : KYNMOBI

    U.S.A
    Bio-Europe Autumn
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    Brand Name : KYNMOBI

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    Bio-Europe Autumn
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    Regulatory Info : DISCN

    Registration Country : USA

    APOMORPHINE HYDROCHLORIDE

    Sumitomo Pharma America

    Dosage Form : FILM;SUBLINGUAL

    Brand Name : KYNMOBI

    Dosage Strength : 20MG

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    Approval Date : 2020-05-21

    Application Number : 210875

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Brand Name : KYNMOBI

    U.S.A
    Bio-Europe Autumn
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    Brand Name : KYNMOBI

    U.S.A
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    Bio-Europe Autumn
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    Regulatory Info : DISCN

    Registration Country : USA

    APOMORPHINE HYDROCHLORIDE

    Sumitomo Pharma America

    Dosage Form : FILM;SUBLINGUAL

    Brand Name : KYNMOBI

    Dosage Strength : 25MG

    Packaging :

    Approval Date : 2020-05-21

    Application Number : 210875

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Brand Name : KYNMOBI

    U.S.A
    Bio-Europe Autumn
    Not Confirmed
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    Brand Name : KYNMOBI

    U.S.A
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    Bio-Europe Autumn
    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    APOMORPHINE HYDROCHLORIDE

    Sumitomo Pharma America

    Dosage Form : FILM;SUBLINGUAL

    Brand Name : KYNMOBI

    Dosage Strength : 30MG

    Packaging :

    Approval Date : 2020-05-21

    Application Number : 210875

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Brand Name : APTIOM

    U.S.A
    Bio-Europe Autumn
    Not Confirmed
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    Brand Name : APTIOM

    U.S.A
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    Bio-Europe Autumn
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    ESLICARBAZEPINE ACETATE

    Sumitomo Pharma America

    Dosage Form : TABLET;ORAL

    Brand Name : APTIOM

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 2013-11-08

    Application Number : 22416

    Regulatory Info : RX

    Registration Country : USA

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    07

    Brand Name : APTIOM

    U.S.A
    Bio-Europe Autumn
    Not Confirmed
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    Brand Name : APTIOM

    U.S.A
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    Bio-Europe Autumn
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    ESLICARBAZEPINE ACETATE

    Sumitomo Pharma America

    Dosage Form : TABLET;ORAL

    Brand Name : APTIOM

    Dosage Strength : 400MG

    Packaging :

    Approval Date : 2013-11-08

    Application Number : 22416

    Regulatory Info : RX

    Registration Country : USA

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    08

    Brand Name : APTIOM

    U.S.A
    Bio-Europe Autumn
    Not Confirmed
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    Brand Name : APTIOM

    U.S.A
    arrow
    Bio-Europe Autumn
    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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    Virtual Booth Virtual Booth
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    Regulatory Info : RX

    Registration Country : USA

    ESLICARBAZEPINE ACETATE

    Sumitomo Pharma America

    Dosage Form : TABLET;ORAL

    Brand Name : APTIOM

    Dosage Strength : 600MG

    Packaging :

    Approval Date : 2013-11-08

    Application Number : 22416

    Regulatory Info : RX

    Registration Country : USA

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    Place

    09

    Brand Name : APTIOM

    U.S.A
    Bio-Europe Autumn
    Not Confirmed
    arrow

    Brand Name : APTIOM

    U.S.A
    arrow
    Bio-Europe Autumn
    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.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
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    Regulatory Info : RX

    Registration Country : USA

    ESLICARBAZEPINE ACETATE

    Sumitomo Pharma America

    Dosage Form : TABLET;ORAL

    Brand Name : APTIOM

    Dosage Strength : 800MG

    Packaging :

    Approval Date : 2013-11-08

    Application Number : 22416

    Regulatory Info : RX

    Registration Country : USA

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    10

    Brand Name : MYFEMBREE

    U.S.A
    Bio-Europe Autumn
    Not Confirmed
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    Brand Name : MYFEMBREE

    U.S.A
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    Bio-Europe Autumn
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    ESTRADIOL; NORETHINDRONE ACETATE; RELUGOLIX

    Sumitomo Pharma America

    Dosage Form : TABLET;ORAL

    Brand Name : MYFEMBREE

    Dosage Strength : 1MG;0.5MG;40MG

    Packaging :

    Approval Date : 2021-05-26

    Application Number : 214846

    Regulatory Info : RX

    Registration Country : USA

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