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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Sunovion Pharmaceuticals

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    01 5LURASIDONE HYDROCHLORIDE

    02 1MITOMYCIN

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    RLD : Yes

    TE Code : AB

    LURASIDONE HYDROCHLORIDE

    Sunovion Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : LATUDA

    Dosage Strength : 40MG

    Approval Date : 2010-10-28

    Application Number : 200603

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    Brand Name : LATUDA

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    RLD : Yes

    TE Code : AB

    LURASIDONE HYDROCHLORIDE

    Sunovion Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : LATUDA

    Dosage Strength : 80MG

    Approval Date : 2010-10-28

    Application Number : 200603

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    Brand Name : LATUDA

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    RLD : Yes

    TE Code : AB

    LURASIDONE HYDROCHLORIDE

    Sunovion Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : LATUDA

    Dosage Strength : 20MG

    Approval Date : 2011-12-07

    Application Number : 200603

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    Brand Name : LATUDA

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    RLD : Yes

    TE Code : AB

    LURASIDONE HYDROCHLORIDE

    Sunovion Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : LATUDA

    Dosage Strength : 120MG

    Approval Date : 2012-04-26

    Application Number : 200603

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    RLD : Yes

    TE Code : AB

    LURASIDONE HYDROCHLORIDE

    Sunovion Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : LATUDA

    Dosage Strength : 60MG

    Approval Date : 2013-07-12

    Application Number : 200603

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    Brand Name : MITOZYTREX

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    RLD : Yes

    TE Code :

    MITOMYCIN

    Sunovion Pharmaceuticals

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : MITOZYTREX

    Dosage Strength : 5MG/VIAL **Federal Regis...

    Approval Date : 2002-11-14

    Application Number : 50763

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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