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    Approved Drug Products containing Velpatasvir listed in the FDA Orange Book. Original Data : FDA Website

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    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

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

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    Velpatasvir

    ACTIVE PHARMA INGREDIENTS

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    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    $ API Ref.Price (USD/KG) : 4,142Xls

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    GILEAD SCIENCES INC

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    RLD : Yes

    TE Code :

    SOFOSBUVIR; VELPATASVIR

    Brand Name : EPCLUSA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 400MG;100MG

    Approval Date : 2016-06-28

    Application Number : 208341

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    RLD : Yes

    TE Code :

    SOFOSBUVIR; VELPATASVIR

    Brand Name : EPCLUSA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 200MG;50MG

    Approval Date : 2020-03-19

    Application Number : 208341

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    RLD : Yes

    TE Code :

    SOFOSBUVIR; VELPATASVIR; VOXILAPREVIR

    Brand Name : VOSEVI

    Dosage Form : TABLET;ORAL

    Dosage Strength : 400MG;100MG;100MG

    Approval Date : 2017-07-18

    Application Number : 209195

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    RLD : Yes

    TE Code :

    SOFOSBUVIR; VELPATASVIR

    Brand Name : EPCLUSA

    Dosage Form : PELLETS;ORAL

    Dosage Strength : 150MG;37.5MG/PACKET

    Approval Date : 2021-06-10

    Application Number : 214187

    RX/OTC/DISCN : RX

    RLD : Yes

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    RLD : Yes

    TE Code :

    SOFOSBUVIR; VELPATASVIR

    Brand Name : EPCLUSA

    Dosage Form : PELLETS;ORAL

    Dosage Strength : 200MG;50MG/PACKET

    Approval Date : 2021-06-10

    Application Number : 214187

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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