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

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    Kikkoman Biochemifa Company advances global health and safety through precision-driven innovation in biotech and food testing.

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    Allsino Pharma excels in R&D & manufacturing of RSMs, GMP intermediates, & APIs; ISO-certified, GMP-compliant, accredited by NMPA.

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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
    Pharmex
    Not Confirmed
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    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Pharmex
    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
    Pharmex
    Not Confirmed
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    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Pharmex
    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 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
    Pharmex
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

    U.S.A
    Pharmex
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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
    Pharmex
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    Brand Name : BREXPIPRAZOLE

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    Pharmex
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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 :

    blank

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    05

    Brand Name : BREXPIPRAZOLE

    U.S.A
    Pharmex
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

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    Pharmex
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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
    Pharmex
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

    U.S.A
    Pharmex
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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
    Pharmex
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

    U.S.A
    Pharmex
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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
    Pharmex
    Not Confirmed
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    Brand Name : BREXPIPRAZOLE

    U.S.A
    Pharmex
    Not Confirmed
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    • fda
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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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    Market
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    09

    Brand Name : CALCITRIOL

    U.S.A
    Pharmex
    Not Confirmed
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    Brand Name : CALCITRIOL

    U.S.A
    Pharmex
    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
    Pharmex
    Not Confirmed
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    Brand Name : CEFDINIR

    U.S.A
    Pharmex
    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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