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    FINISHED DOSAGE FORMULATIONS

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    01 2AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    02 6BREXPIPRAZOLE

    03 1CALCITRIOL

    04 3CEFDINIR

    05 2CEFPODOXIME PROXETIL

    06 1CEFTRIAXONE SODIUM

    07 3CEFUROXIME AXETIL

    08 2CEPHALEXIN

    09 2CLOBAZAM

    10 2CYCLOBENZAPRINE HYDROCHLORIDE

    11 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    12 1FLUOCINOLONE ACETONIDE

    13 4HYDRALAZINE HYDROCHLORIDE

    14 2LEVETIRACETAM

    15 3LEVOFLOXACIN

    16 1LORATADINE

    17 3LORAZEPAM

    18 2MELOXICAM

    19 2METHYLPHENIDATE HYDROCHLORIDE

    20 2OMEPRAZOLE; SODIUM BICARBONATE

    21 2POTASSIUM CHLORIDE

    22 1PREGABALIN

    23 2PRIMIDONE

    24 3SERTRALINE HYDROCHLORIDE

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    01

    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Process Development
    Not Confirmed
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    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Process Development
    Not Confirmed
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    RLD : No

    TE Code :

    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CHLORDIAZEPOXIDE AND AMI...

    Dosage Strength : EQ 12.5MG BASE;5MG

    Approval Date : 1986-12-10

    Application Number : 70765

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    02

    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Process Development
    Not Confirmed
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    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
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    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CHLORDIAZEPOXIDE AND AMI...

    Dosage Strength : EQ 25MG BASE;10MG

    Approval Date : 1986-12-10

    Application Number : 70766

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    03

    Brand Name : BREXPIPRAZOLE

    U.S.A
    Process Development
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

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    RLD : No

    TE Code :

    BREXPIPRAZOLE

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : BREXPIPRAZOLE

    Dosage Strength : 0.25MG

    Approval Date : 2023-10-25

    Application Number : 213758

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    04

    Brand Name : BREXPIPRAZOLE

    U.S.A
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    Brand Name : BREXPIPRAZOLE

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    RLD : No

    TE Code :

    BREXPIPRAZOLE

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : BREXPIPRAZOLE

    Dosage Strength : 0.5MG

    Approval Date : 2023-10-25

    Application Number : 213758

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : BREXPIPRAZOLE

    U.S.A
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    Brand Name : BREXPIPRAZOLE

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    RLD : No

    TE Code :

    BREXPIPRAZOLE

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : BREXPIPRAZOLE

    Dosage Strength : 1MG

    Approval Date : 2023-10-25

    Application Number : 213758

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    06

    Brand Name : BREXPIPRAZOLE

    U.S.A
    Process Development
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

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    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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    RLD : No

    TE Code :

    BREXPIPRAZOLE

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : BREXPIPRAZOLE

    Dosage Strength : 2MG

    Approval Date : 2023-10-25

    Application Number : 213758

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    Brand Name : BREXPIPRAZOLE

    U.S.A
    Process Development
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

    U.S.A
    Process Development
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    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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    RLD : No

    TE Code :

    BREXPIPRAZOLE

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : BREXPIPRAZOLE

    Dosage Strength : 3MG

    Approval Date : 2023-10-25

    Application Number : 213758

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    08

    Brand Name : BREXPIPRAZOLE

    U.S.A
    Process Development
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

    U.S.A
    Process Development
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    RLD : No

    TE Code :

    BREXPIPRAZOLE

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : BREXPIPRAZOLE

    Dosage Strength : 4MG

    Approval Date : 2023-10-25

    Application Number : 213758

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    Brand Name : CALCITRIOL

    U.S.A
    Process Development
    Not Confirmed
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    Brand Name : CALCITRIOL

    U.S.A
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    Not Confirmed
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    RLD : No

    TE Code : AA

    CALCITRIOL

    ANDA Repository

    Dosage Form : SOLUTION; ORAL

    Proprietary Name : CALCITRIOL

    Dosage Strength : 1MCG/ML

    Approval Date : 2023-07-28

    Application Number : 203973

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AA

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    10

    Brand Name : CEFDINIR

    U.S.A
    Process Development
    Not Confirmed
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    Brand Name : CEFDINIR

    U.S.A
    Process Development
    Not Confirmed
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    RLD : No

    TE Code : AB

    CEFDINIR

    ANDA Repository

    Dosage Form : CAPSULE; ORAL

    Proprietary Name : CEFDINIR

    Dosage Strength : 300MG

    Approval Date : 2007-07-18

    Application Number : 65418

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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