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    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

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    FINISHED DOSAGE FORMULATIONS

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    01 2AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE

    02 1CALCITRIOL

    03 3CEFDINIR

    04 2CEFPODOXIME PROXETIL

    05 1CEFTRIAXONE SODIUM

    06 3CEFUROXIME AXETIL

    07 2CEPHALEXIN

    08 2CYCLOBENZAPRINE HYDROCHLORIDE

    09 1DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM

    10 1FLUOCINOLONE ACETONIDE

    11 4HYDRALAZINE HYDROCHLORIDE

    12 2LEVETIRACETAM

    13 1LORATADINE

    14 3LORAZEPAM

    15 2MELOXICAM

    16 2METHYLPHENIDATE HYDROCHLORIDE

    17 2OMEPRAZOLE; SODIUM BICARBONATE

    18 3POTASSIUM CHLORIDE

    19 1PREGABALIN

    20 2PRIMIDONE

    21 3SERTRALINE HYDROCHLORIDE

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    01

    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Organic Process R&D
    Not Confirmed
    arrow
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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 :

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    02

    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Brand Name : CHLORDIAZEPOXIDE AND...

    U.S.A
    Organic Process R&D
    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 :

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    03

    Brand Name : CALCITRIOL

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Brand Name : CALCITRIOL

    U.S.A
    Organic Process R&D
    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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    04

    Brand Name : CEFDINIR

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Brand Name : CEFDINIR

    U.S.A
    Organic Process R&D
    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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    05

    Brand Name : CEFDINIR

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Brand Name : CEFDINIR

    U.S.A
    Organic Process R&D
    Not Confirmed
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    RLD : No

    TE Code : AB

    CEFDINIR

    ANDA Repository

    Dosage Form : FOR SUSPENSION; ORAL

    Proprietary Name : CEFDINIR

    Dosage Strength : 125MG/5ML

    Approval Date : 2007-07-18

    Application Number : 65429

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    06

    Brand Name : CEFDINIR

    U.S.A
    Organic Process R&D
    Not Confirmed
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    Brand Name : CEFDINIR

    U.S.A
    Organic Process R&D
    Not Confirmed
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    RLD : No

    TE Code : AB

    CEFDINIR

    ANDA Repository

    Dosage Form : FOR SUSPENSION; ORAL

    Proprietary Name : CEFDINIR

    Dosage Strength : 250MG/5ML

    Approval Date : 2007-07-18

    Application Number : 65429

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : CEFPODOXIME PROXETIL

    U.S.A
    Organic Process R&D
    Not Confirmed
    arrow

    Brand Name : CEFPODOXIME PROXETIL

    U.S.A
    Organic Process R&D
    Not Confirmed
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    RLD : No

    TE Code : AB

    CEFPODOXIME PROXETIL

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFPODOXIME PROXETIL

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2007-11-14

    Application Number : 65388

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    Brand Name : CEFPODOXIME PROXETIL

    U.S.A
    Organic Process R&D
    Not Confirmed
    arrow

    Brand Name : CEFPODOXIME PROXETIL

    U.S.A
    Organic Process R&D
    Not Confirmed
    arrow
    • fda
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    RLD : No

    TE Code : AB

    CEFPODOXIME PROXETIL

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFPODOXIME PROXETIL

    Dosage Strength : EQ 200MG BASE

    Approval Date : 2007-11-14

    Application Number : 65388

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : CEFTRIAXONE SODIUM

    U.S.A
    Organic Process R&D
    Not Confirmed
    arrow

    Brand Name : CEFTRIAXONE SODIUM

    U.S.A
    Organic Process R&D
    Not Confirmed
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    RLD : No

    TE Code : AP

    CEFTRIAXONE SODIUM

    ANDA Repository

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : CEFTRIAXONE SODIUM

    Dosage Strength : EQ 10GM BASE/VIAL

    Approval Date : 2017-01-20

    Application Number : 91117

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AP

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    10

    Brand Name : CEFUROXIME AXETIL

    U.S.A
    Organic Process R&D
    Not Confirmed
    arrow

    Brand Name : CEFUROXIME AXETIL

    U.S.A
    Organic Process R&D
    Not Confirmed
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    • fda
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    RLD : No

    TE Code : AB

    CEFUROXIME AXETIL

    ANDA Repository

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFUROXIME AXETIL

    Dosage Strength : EQ 125MG BASE

    Approval Date : 2008-02-15

    Application Number : 65359

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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