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

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    Regulatory Info : Marketed

    Registration Country : Norway

    Nonacog beta pegol

    Brand Name : Refixia

    Dosage Form : Solution For Injection

    Dosage Strength : 1000IU

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    Regulatory Info : Marketed

    Registration Country : Norway

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    Regulatory Info : Marketed

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    Nonacog beta pegol

    Brand Name : Refixia

    Dosage Form : Solution For Injection

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    Regulatory Info : Marketed

    Registration Country : Norway

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    Regulatory Info : Authorized

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    Nonacog Beta Pegol

    Brand Name : Refixia

    Dosage Form : Powder And Solvent For Injectable Solution

    Dosage Strength : 1000IU

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    Approval Date : 11-12-2017

    Application Number : 1171193002

    Regulatory Info : Authorized

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    Regulatory Info : Authorized

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    Nonacog Beta Pegol

    Brand Name : Refixia

    Dosage Form : Powder And Solvent For Injectable Solution

    Dosage Strength : 3000IU

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    Approval Date : 23-03-2023

    Application Number : 1171193004

    Regulatory Info : Authorized

    Registration Country : Spain

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    05

    Novo Nordisk A/S

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    Regulatory Info : Authorized

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    Nonacog Beta Pegol

    Brand Name : Refixia

    Dosage Form : Powder And Solvent For Injectable Solution

    Dosage Strength : 500IU

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    Approval Date : 11-12-2017

    Application Number : 1171193001

    Regulatory Info : Authorized

    Registration Country : Spain

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    Novo Nordisk A/S

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    Regulatory Info : Authorized

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    Nonacog Beta Pegol

    Brand Name : Refixia

    Dosage Form : Powder And Solvent For Injectable Solution

    Dosage Strength : 2000IU

    Packaging :

    Approval Date : 11-12-2017

    Application Number : 1171193003

    Regulatory Info : Authorized

    Registration Country : Spain

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    07

    Novo Nordisk A/S

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    Regulatory Info : Approved

    Registration Country : Sweden

    Nonakog Beta Pegol

    Brand Name : Refixia

    Dosage Form : Solution For Injection

    Dosage Strength : 500IU

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    Approval Date : 02-06-2017

    Application Number : 2.02E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    08

    Novo Nordisk A/S

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    PEGS Boston Summit
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    Regulatory Info : Approved

    Registration Country : Sweden

    Nonakog Beta Pegol

    Brand Name : Refixia

    Dosage Form : Solution For Injection

    Dosage Strength : 1000IE

    Packaging :

    Approval Date : 02-06-2017

    Application Number : 2.02E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    09

    Novo Nordisk A/S

    Denmark
    PEGS Boston Summit
    Not Confirmed
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    Novo Nordisk A/S

    Denmark
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    PEGS Boston Summit
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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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    Regulatory Info : Approved

    Registration Country : Sweden

    Nonakog Beta Pegol

    Brand Name : Refixia

    Dosage Form : Solution For Injection

    Dosage Strength : 2000IE

    Packaging :

    Approval Date : 02-06-2017

    Application Number : 2.02E+13

    Regulatory Info : Approved

    Registration Country : Sweden

    blank

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    10

    Novo Nordisk A/S

    Denmark
    PEGS Boston Summit
    Not Confirmed
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    Novo Nordisk A/S

    Denmark
    arrow
    PEGS Boston Summit
    Not Confirmed
    • 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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    Flag Denmark
    Virtual Booth Virtual Booth
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    Regulatory Info : Approved

    Registration Country : Sweden

    Nonakog Beta Pegol

    Brand Name : Refixia

    Dosage Form : Solution For Injection

    Dosage Strength : 3000IU

    Packaging :

    Approval Date : 12-12-2022

    Application Number : 2.02E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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