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    RLD :

    TE Code :

    BREXPIPRAZOLE

    Brand Name : BREXPIPRAZOLE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.25MG

    Approval Date :

    Application Number : 213477

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    TE Code :

    Biophore CB

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    RLD :

    TE Code :

    BREXPIPRAZOLE

    Brand Name : BREXPIPRAZOLE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

    Approval Date :

    Application Number : 213477

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    TE Code :

    BREXPIPRAZOLE

    Brand Name : BREXPIPRAZOLE

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    Dosage Strength : 1MG

    Approval Date :

    Application Number : 213477

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    RLD :

    TE Code :

    BREXPIPRAZOLE

    Brand Name : BREXPIPRAZOLE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Approval Date :

    Application Number : 213477

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    TE Code :

    BREXPIPRAZOLE

    Brand Name : BREXPIPRAZOLE

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    Dosage Strength : 3MG

    Approval Date :

    Application Number : 213477

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    RLD :

    TE Code :

    BREXPIPRAZOLE

    Brand Name : BREXPIPRAZOLE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 4MG

    Approval Date :

    Application Number : 213477

    RX/OTC/DISCN :

    RLD :

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    Biophore CB

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    RLD : Yes

    TE Code : AB

    BREXPIPRAZOLE

    Brand Name : REXULTI

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.25MG

    Approval Date : 2015-07-10

    Application Number : 205422

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    RLD : Yes

    TE Code : AB

    BREXPIPRAZOLE

    Brand Name : REXULTI

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.5MG

    Approval Date : 2015-07-10

    Application Number : 205422

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    RLD : Yes

    TE Code : AB

    BREXPIPRAZOLE

    Brand Name : REXULTI

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Approval Date : 2015-07-10

    Application Number : 205422

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    OTSUKA

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    RLD : Yes

    TE Code : AB

    BREXPIPRAZOLE

    Brand Name : REXULTI

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2MG

    Approval Date : 2015-07-10

    Application Number : 205422

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

    blank

    Portfolio PDF

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