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    Suanfarma, at the Core of a Better Life.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.

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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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    CEPHALON INC

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    Brand Name : NUVIGIL

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    Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2009-03-26

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    CEPHALON INC

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    Approval Date : 2007-06-15

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    CEPHALON INC

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    Brand Name : NUVIGIL

    Dosage Form : TABLET;ORAL

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    Approval Date : 2009-03-26

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    CorePharma, LLC

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    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

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    Approval Date : 2019-03-25

    Application Number : 201514

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    CorePharma, LLC

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    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

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    Approval Date : 2019-03-25

    Application Number : 201514

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    13

    CorePharma, LLC

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    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 250MG

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    Approval Date : 2019-03-25

    Application Number : 201514

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    14

    Lupin Ltd

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    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

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    Approval Date : 2016-11-28

    Application Number : 200751

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    Lupin Ltd

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    Lupin Ltd

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    Approval Date : 2016-11-28

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    Lupin Ltd

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    Brand Name : ARMODAFINIL

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    Approval Date : 2016-11-28

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    18

    Lupin Ltd

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    Approval Date : 2016-11-28

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    Natco Pharma

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    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 50MG

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    Approval Date : 2016-11-28

    Application Number : 202768

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    Natco Pharma

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    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 150MG

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    Approval Date : 2016-11-28

    Application Number : 202768

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    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
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    Brand Name : ARMODAFINIL

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    Application Number : 200152

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    Teva Pharmaceutical Industries

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    Brand Name : ARMODAFINIL

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    Teva Pharmaceutical Industries

    Israel
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    Brand Name : ARMODAFINIL

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    Teva Pharmaceutical Industries

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    Teva Pharmaceutical Industries

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    Viatris

    U.S.A
    Cosmoprof
    Not Confirmed
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    Viatris

    U.S.A
    arrow
    Cosmoprof
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    ARMODAFINIL

    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 2012-06-01

    Application Number : 200043

    Regulatory Info : RX

    Registration Country : USA

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    27

    Viatris

    U.S.A
    Cosmoprof
    Not Confirmed
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    Viatris

    U.S.A
    arrow
    Cosmoprof
    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
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    ARMODAFINIL

    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 150MG

    Packaging :

    Approval Date : 2012-06-01

    Application Number : 200043

    Regulatory Info : RX

    Registration Country : USA

    blank

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    28

    Viatris

    U.S.A
    Cosmoprof
    Not Confirmed
    arrow

    Viatris

    U.S.A
    arrow
    Cosmoprof
    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
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    ARMODAFINIL

    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 250MG

    Packaging :

    Approval Date : 2012-06-01

    Application Number : 200043

    Regulatory Info : RX

    Registration Country : USA

    blank

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    29

    Viatris

    U.S.A
    Cosmoprof
    Not Confirmed
    arrow

    Viatris

    U.S.A
    arrow
    Cosmoprof
    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
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    ARMODAFINIL

    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Packaging :

    Approval Date : 2019-05-09

    Application Number : 200043

    Regulatory Info : RX

    Registration Country : USA

    blank

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    Virtual Booth

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    30

    Viatris

    U.S.A
    Cosmoprof
    Not Confirmed
    arrow

    Viatris

    U.S.A
    arrow
    Cosmoprof
    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
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    ARMODAFINIL

    Brand Name : ARMODAFINIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 200MG

    Packaging :

    Approval Date : 2019-05-09

    Application Number : 200043

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF