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    VKT Pharma

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    01 2FAMOTIDINE

    02 2RANITIDINE HYDROCHLORIDE

    03 2RANOLAZINE

    04 3SUMATRIPTAN SUCCINATE

    05 4TADALAFIL

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    Brand Name : FAMOTIDINE

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    RLD : No

    TE Code :

    FAMOTIDINE

    VKT Pharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : FAMOTIDINE

    Dosage Strength : 10MG

    Approval Date : 2022-01-28

    Application Number : 215822

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    02

    Brand Name : FAMOTIDINE

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    RLD : No

    TE Code :

    FAMOTIDINE

    VKT Pharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : FAMOTIDINE

    Dosage Strength : 20MG

    Approval Date : 2022-01-28

    Application Number : 215822

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    03

    Brand Name : RANITIDINE HYDROCHLO...

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    RLD : No

    TE Code : AB

    RANITIDINE HYDROCHLORIDE

    VKT Pharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : RANITIDINE HYDROCHLORIDE

    Dosage Strength : EQ 150MG BASE

    Approval Date : 2019-01-31

    Application Number : 211289

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : RANITIDINE HYDROCHLO...

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    RLD : No

    TE Code : AB

    RANITIDINE HYDROCHLORIDE

    VKT Pharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : RANITIDINE HYDROCHLORIDE

    Dosage Strength : EQ 300MG BASE

    Approval Date : 2019-01-31

    Application Number : 211289

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    05

    Brand Name : RANOLAZINE

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    RLD : No

    TE Code : AB

    RANOLAZINE

    VKT Pharma

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : RANOLAZINE

    Dosage Strength : 500MG

    Approval Date : 2022-01-19

    Application Number : 214035

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    RLD : No

    TE Code : AB

    RANOLAZINE

    VKT Pharma

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : RANOLAZINE

    Dosage Strength : 1GM

    Approval Date : 2022-01-19

    Application Number : 214035

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    07

    Brand Name : SUMATRIPTAN SUCCINAT...

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    Brand Name : SUMATRIPTAN SUCCINAT...

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    RLD : No

    TE Code : AB

    SUMATRIPTAN SUCCINATE

    VKT Pharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : SUMATRIPTAN SUCCINATE

    Dosage Strength : EQ 25MG BASE

    Approval Date : 2024-12-31

    Application Number : 219036

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    08

    Brand Name : SUMATRIPTAN SUCCINAT...

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    Brand Name : SUMATRIPTAN SUCCINAT...

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    RLD : No

    TE Code : AB

    SUMATRIPTAN SUCCINATE

    VKT Pharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : SUMATRIPTAN SUCCINATE

    Dosage Strength : EQ 50MG BASE

    Approval Date : 2024-12-31

    Application Number : 219036

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    09

    Brand Name : SUMATRIPTAN SUCCINAT...

    India
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    Not Confirmed
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    Brand Name : SUMATRIPTAN SUCCINAT...

    India
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    • fda
    • EDQM
    • WHO-GMP
    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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    Virtual Booth Virtual Booth
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    RLD : No

    TE Code : AB

    SUMATRIPTAN SUCCINATE

    VKT Pharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : SUMATRIPTAN SUCCINATE

    Dosage Strength : EQ 100MG BASE

    Approval Date : 2024-12-31

    Application Number : 219036

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    10

    Brand Name : TADALAFIL

    India
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    Brand Name : TADALAFIL

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    • fda
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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 : AB1

    TADALAFIL

    VKT Pharma

    Dosage Form : TABLET; ORAL

    Proprietary Name : TADALAFIL

    Dosage Strength : 2.5MG

    Approval Date : 2021-11-04

    Application Number : 215556

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB1

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