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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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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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    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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    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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    06

    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 : 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...

    India
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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
    Florida Innovation
    Not Confirmed
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    Brand Name : SUMATRIPTAN SUCCINAT...

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    • fda
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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
    Florida Innovation
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    Brand Name : TADALAFIL

    India
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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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