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    Approved Drug Products containing 1-(3-(Dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile hydrobromide listed in the FDA Orange Book. Original Data : FDA Website

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    Renejix: CDMO with expertise in small molecule oral dosage, delivery tech, and multi-modality manufacturing.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    xyz-pharma-m-2024-10-07

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    Ribobay has expertise in oligonucleotides from siRNA, Antisense Oligonucleotides, miRNAs, and aptamers & Oligonucleotides CXOs.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    xyz-pharma-m-2024-10-07

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    1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile Hydrobromide

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    01 4ABBVIE

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    01

    ABBVIE

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    RLD : Yes

    TE Code : AB

    CITALOPRAM HYDROBROMIDE

    Brand Name : CELEXA

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2000-04-27

    Application Number : 20822

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    ABBVIE

    U.S.A
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    RLD : Yes

    TE Code : AB

    CITALOPRAM HYDROBROMIDE

    Brand Name : CELEXA

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Approval Date : 1998-07-17

    Application Number : 20822

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    03

    ABBVIE

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    RLD : Yes

    TE Code : AB

    CITALOPRAM HYDROBROMIDE

    Brand Name : CELEXA

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Approval Date : 1998-07-17

    Application Number : 20822

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    ABBVIE

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    RLD : No

    TE Code :

    CITALOPRAM HYDROBROMIDE

    Brand Name : CELEXA

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 60MG BASE

    Approval Date : 1998-07-17

    Application Number : 20822

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    TARO

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    RLD : No

    TE Code :

    CITALOPRAM HYDROBROMIDE

    Brand Name : CITALOPRAM HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2006-03-22

    Application Number : 77278

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    TARO

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    RLD : No

    TE Code :

    CITALOPRAM HYDROBROMIDE

    Brand Name : CITALOPRAM HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2006-03-22

    Application Number : 77278

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    TARO

    U.S.A
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    RLD : No

    TE Code :

    CITALOPRAM HYDROBROMIDE

    Brand Name : CITALOPRAM HYDROBROMIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 40MG BASE

    Approval Date : 2006-03-22

    Application Number : 77278

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    08

    BIOVAIL LABS INTL

    Canada
    AAPS 2024
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    BIOVAIL LABS INTL

    Canada
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    RLD : Yes

    TE Code :

    CITALOPRAM HYDROBROMIDE

    Brand Name : CITALOPRAM HYDROBROMIDE

    Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2005-12-20

    Application Number : 21763

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    09

    BIOVAIL LABS INTL

    Canada
    AAPS 2024
    Not Confirmed
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    BIOVAIL LABS INTL

    Canada
    arrow
    AAPS 2024
    Not Confirmed
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    RLD : Yes

    TE Code :

    CITALOPRAM HYDROBROMIDE

    Brand Name : CITALOPRAM HYDROBROMIDE

    Dosage Form : TABLET, ORALLY DISINTEGRATING;ORAL

    Dosage Strength : EQ 20MG BASE

    Approval Date : 2005-12-20

    Application Number : 21763

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

    blank

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    10

    FOREST LABS

    U.S.A
    AAPS 2024
    Not Confirmed
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    FOREST LABS

    U.S.A
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    AAPS 2024
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    RLD : Yes

    TE Code :

    CITALOPRAM HYDROBROMIDE

    Brand Name : CELEXA

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : EQ 10MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1999-12-22

    Application Number : 21046

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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