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    Noven Pharmaceuticals

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    01 4DEXTROAMPHETAMINE

    02 5ESTRADIOL

    03 2ESTRADIOL; NORETHINDRONE ACETATE

    04 4FENTANYL

    05 3LIDOCAINE

    06 3LITHIUM CARBONATE

    07 4METHYLPHENIDATE

    08 3NITROGLYCERIN

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    01

    Brand Name : XELSTRYM

    U.S.A
    2024 ACI Convention
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    Brand Name : XELSTRYM

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    RLD : Yes

    TE Code :

    DEXTROAMPHETAMINE

    Noven Pharmaceuticals

    Dosage Form : SYSTEM; TRANSDERMAL

    Proprietary Name : XELSTRYM

    Dosage Strength : 4.5MG/9HR

    Approval Date : 2022-03-22

    Application Number : 215401

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : XELSTRYM

    U.S.A
    2024 ACI Convention
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    Brand Name : XELSTRYM

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    RLD : Yes

    TE Code :

    DEXTROAMPHETAMINE

    Noven Pharmaceuticals

    Dosage Form : SYSTEM; TRANSDERMAL

    Proprietary Name : XELSTRYM

    Dosage Strength : 9MG/9HR

    Approval Date : 2022-03-22

    Application Number : 215401

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : XELSTRYM

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    RLD : Yes

    TE Code :

    DEXTROAMPHETAMINE

    Noven Pharmaceuticals

    Dosage Form : SYSTEM; TRANSDERMAL

    Proprietary Name : XELSTRYM

    Dosage Strength : 13.5MG/9HR

    Approval Date : 2022-03-22

    Application Number : 215401

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : XELSTRYM

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    RLD : Yes

    TE Code :

    DEXTROAMPHETAMINE

    Noven Pharmaceuticals

    Dosage Form : SYSTEM; TRANSDERMAL

    Proprietary Name : XELSTRYM

    Dosage Strength : 18MG/9HR

    Approval Date : 2022-03-22

    Application Number : 215401

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    05

    Brand Name : MINIVELLE

    U.S.A
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    RLD : Yes

    TE Code : AB3

    ESTRADIOL

    Noven Pharmaceuticals

    Dosage Form : FILM, EXTENDED RELEASE; TRANSD...

    Proprietary Name : MINIVELLE

    Dosage Strength : 0.0375MG/24HR

    Approval Date : 2012-10-29

    Application Number : 203752

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB3

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    06

    Brand Name : MINIVELLE

    U.S.A
    2024 ACI Convention
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    RLD : Yes

    TE Code : AB3

    ESTRADIOL

    Noven Pharmaceuticals

    Dosage Form : FILM, EXTENDED RELEASE; TRANSD...

    Proprietary Name : MINIVELLE

    Dosage Strength : 0.075MG/24HR

    Approval Date : 2012-10-29

    Application Number : 203752

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB3

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    07

    Brand Name : MINIVELLE

    U.S.A
    2024 ACI Convention
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    Brand Name : MINIVELLE

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    RLD : Yes

    TE Code : AB3

    ESTRADIOL

    Noven Pharmaceuticals

    Dosage Form : FILM, EXTENDED RELEASE; TRANSD...

    Proprietary Name : MINIVELLE

    Dosage Strength : 0.05MG/24HR

    Approval Date : 2012-10-29

    Application Number : 203752

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB3

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    08

    Brand Name : MINIVELLE

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : MINIVELLE

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    RLD : Yes

    TE Code : AB3

    ESTRADIOL

    Noven Pharmaceuticals

    Dosage Form : FILM, EXTENDED RELEASE; TRANSD...

    Proprietary Name : MINIVELLE

    Dosage Strength : 0.1MG/24HR

    Approval Date : 2012-10-29

    Application Number : 203752

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB3

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    09

    Brand Name : MINIVELLE

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : MINIVELLE

    U.S.A
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    RLD : Yes

    TE Code : AB3

    ESTRADIOL

    Noven Pharmaceuticals

    Dosage Form : FILM, EXTENDED RELEASE; TRANSD...

    Proprietary Name : MINIVELLE

    Dosage Strength : 0.025MG/24HR

    Approval Date : 2014-09-23

    Application Number : 203752

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB3

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    10

    Brand Name : COMBIPATCH

    U.S.A
    2024 ACI Convention
    Not Confirmed
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    Brand Name : COMBIPATCH

    U.S.A
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    RLD : Yes

    TE Code :

    ESTRADIOL; NORETHINDRONE ACETATE

    Noven Pharmaceuticals

    Dosage Form : FILM, EXTENDED RELEASE; TRANSD...

    Proprietary Name : COMBIPATCH

    Dosage Strength : 0.05MG/24HR;0.14MG/24HR

    Approval Date : 1998-08-07

    Application Number : 20870

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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