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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Evonik Health Care is the innovation hub for leading life science companies

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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Bictegravir Sodium

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    01

    Gilead Sciences

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    Regulatory Info : RX

    Registration Country : USA

    BICTEGRAVIR SODIUM; EMTRICITABINE; TENOFOVIR ALAFENAMIDE FUMARATE

    Brand Name : BIKTARVY

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 50MG BASE;200MG;EQ 25MG BASE

    Packaging :

    Approval Date : 2018-02-07

    Application Number : 210251

    Regulatory Info : RX

    Registration Country : USA

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    02

    Gilead Sciences

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    Regulatory Info : RX

    Registration Country : USA

    BICTEGRAVIR SODIUM; EMTRICITABINE; TENOFOVIR ALAFENAMIDE FUMARATE

    Brand Name : BIKTARVY

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 30MG BASE;120MG;EQ 15MG BASE

    Packaging :

    Approval Date : 2021-10-07

    Application Number : 210251

    Regulatory Info : RX

    Registration Country : USA

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    03

    Gilead Sciences

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    Regulatory Info : Approved

    Registration Country : Sweden

    Bictegravir Sodium; Emtricitabine; Tenofovir Alafenamide Hemifumarate

    Brand Name : Confessional View

    Dosage Form : Film Coated Tablet

    Dosage Strength : 30mg;120mg;15mg

    Packaging :

    Approval Date : 21/11/2022

    Application Number : 20210531000118

    Regulatory Info : Approved

    Registration Country : Sweden

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    04

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    Regulatory Info : Approved

    Registration Country : Sweden

    Bictegravir Sodium; Emtricitabine; Tenofovir Alafenamide Hemifumarate

    Brand Name : Confessional View

    Dosage Form : Film Coated Tablet

    Dosage Strength : 50mg;200mg;25mg

    Packaging :

    Approval Date : 21/06/2018

    Application Number : 20170622000024

    Regulatory Info : Approved

    Registration Country : Sweden

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    05

    Gilead Sciences

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    Regulatory Info : Authorized

    Registration Country : Spain

    Emtricitabine; Tenofovir Alafenamide Fumarate; Bictegravir Sodium

    Brand Name : Biktarvy

    Dosage Form : Film Coated Tablet

    Dosage Strength : 50MG; 200MG; 25 MG

    Packaging :

    Approval Date : 17-05-2022

    Application Number : 181289001IP

    Regulatory Info : Authorized

    Registration Country : Spain

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    06

    Gilead Sciences

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    Regulatory Info : Authorized

    Registration Country : Spain

    Emtricitabine; Tenofovir Alafenamide Fumarate; Bictegravir Sodium

    Brand Name : Biktarvy

    Dosage Form : Film Coated Tablet

    Dosage Strength : 50MG; 200MG; 25 MG

    Packaging :

    Approval Date : 10-07-2018

    Application Number : 1181289001

    Regulatory Info : Authorized

    Registration Country : Spain

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    07

    Gilead Sciences

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    Regulatory Info : Prescription

    Registration Country : Canada

    BICTEGRAVIR (BICTEGRAVIR SODIUM)

    Brand Name : BIKTARVY

    Dosage Form : TABLET

    Dosage Strength : 50MG

    Packaging : 30

    Approval Date :

    Application Number : 2478579

    Regulatory Info : Prescription

    Registration Country : Canada

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    08

    Gilead Sciences

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    Regulatory Info : Prescription

    Registration Country : Denmark

    Bictegravir Sodium; Emtricitabin; Tenofovir Alafenamide Fumarate

    Brand Name : Biktarvy

    Dosage Form : Film Coated Tablet

    Dosage Strength : 30mg; 120mg; 15mg

    Packaging :

    Approval Date : 21-11-2022

    Application Number : 28106641421

    Regulatory Info : Prescription

    Registration Country : Denmark

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    09

    Gilead Sciences

    U.S.A
    ASPEN
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    Gilead Sciences

    U.S.A
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    ASPEN
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    Regulatory Info : Prescription

    Registration Country : Denmark

    Bictegravir Sodium; Emtricitabin; Tenofovir Alafenamide

    Brand Name : Biktarvy

    Dosage Form : Film Coated Tablet

    Dosage Strength : 50mg; 200mg; 25mg

    Packaging :

    Approval Date : 21-06-2018

    Application Number : 28105970117

    Regulatory Info : Prescription

    Registration Country : Denmark

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.