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

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    pharmacompass-1-m-2026-01-12

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    End-to-end drug development, specializing in high-potency softgels and liquids, providing global partners with a competitive advantage.

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    Kewpie is your partner for Sodium Hyaluronate & Hyaluronic Acid// CEP, USDMF, KDMF & JDMF registered.

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    pharmacompass-2-m-2025-11-03

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    01 2Amlodipine Maleate

    02 1Azacitidin

    03 1Azacitidine

    04 3Hydrochlorthiazide Quinapril Hydrochloride

    05 4Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride

    06 4Torasemide (Anhydrous)

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    01

    Brand Name : Amlodipine Tad

    Germany
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    Brand Name : Amlodipine Tad

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Amlodipine Maleate

    Betapharm Arzneimittel

    Dosage Form : Tablet

    Brand Name : Amlodipine Tad

    Dosage Strength : 10mg

    Packaging :

    Approval Date : 23/05/2003

    Application Number : 20030523000113

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    02

    Brand Name : Amlodipine Tad

    Germany
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    Brand Name : Amlodipine Tad

    Germany
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Amlodipine Maleate

    Betapharm Arzneimittel

    Dosage Form : Tablet

    Brand Name : Amlodipine Tad

    Dosage Strength : 5mg

    Packaging :

    Approval Date : 23/05/2003

    Application Number : 20030523000106

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    03

    Brand Name : Azacitidine betaphar...

    Germany
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    Regulatory Info : Marketed

    Registration Country : Norway

    Azacitidin

    Betapharm Arzneimittel

    Dosage Form : Injectable Solution

    Brand Name : Azacitidine betapharm

    Dosage Strength : 25mg/ml

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    Regulatory Info : Marketed

    Registration Country : Norway

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    04

    Brand Name : Azacitidine Betaphar...

    Germany
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    Regulatory Info : Approved

    Registration Country : Sweden

    Azacitidine

    Betapharm Arzneimittel

    Dosage Form : Solution For Injection

    Brand Name : Azacitidine Betapharm

    Dosage Strength : 25mg/ml

    Packaging :

    Approval Date : 24/03/2020

    Application Number : 20190110000022

    Regulatory Info : Approved

    Registration Country : Sweden

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    05

    Brand Name : Kiprimed Comp

    Germany
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    Brand Name : Kiprimed Comp

    Germany
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Hydrochlorthiazide Quinapril Hydrochloride

    Betapharm Arzneimittel

    Dosage Form : Film Coated Tablet

    Brand Name : Kiprimed Comp

    Dosage Strength : 10mg;12.5mg

    Packaging :

    Approval Date : 30/04/2004

    Application Number : 20040430000083

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    06

    Brand Name : Kiprimed Comp

    Germany
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    Brand Name : Kiprimed Comp

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Hydrochlorthiazide Quinapril Hydrochloride

    Betapharm Arzneimittel

    Dosage Form : Film Coated Tablet

    Brand Name : Kiprimed Comp

    Dosage Strength : 20mg;12.5mg

    Packaging :

    Approval Date : 30/04/2004

    Application Number : 20040430000090

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    07

    Brand Name : Kiprimed Comp

    Germany
    VMX
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    Brand Name : Kiprimed Comp

    Germany
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Hydrochlorthiazide Quinapril Hydrochloride

    Betapharm Arzneimittel

    Dosage Form : Film Coated Tablet

    Brand Name : Kiprimed Comp

    Dosage Strength : 20mg;25mg

    Packaging :

    Approval Date : 30/04/2004

    Application Number : 20040430000106

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    08

    Brand Name : Oxycodone/Naloxone B...

    Germany
    VMX
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    Brand Name : Oxycodone/Naloxone B...

    Germany
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride

    Betapharm Arzneimittel

    Dosage Form : Tablet

    Brand Name : Oxycodone/Naloxone Betaph...

    Dosage Strength : 10mg;5mg

    Packaging :

    Approval Date : 22/06/2016

    Application Number : 20141118000026

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    09

    Brand Name : Oxycodone/Naloxone B...

    Germany
    VMX
    Not Confirmed
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    Brand Name : Oxycodone/Naloxone B...

    Germany
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    VMX
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride

    Betapharm Arzneimittel

    Dosage Form : Tablet

    Brand Name : Oxycodone/Naloxone Betaph...

    Dosage Strength : 20mg;10mg

    Packaging :

    Approval Date : 22/06/2016

    Application Number : 20141118000033

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    10

    Brand Name : Oxycodone/Naloxone B...

    Germany
    VMX
    Not Confirmed
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    Brand Name : Oxycodone/Naloxone B...

    Germany
    arrow
    VMX
    Not Confirmed
    • 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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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : Deregistered

    Registration Country : Sweden

    Naloxone Hydrochloride Dihydrate; Oxycodone Hydrochloride

    Betapharm Arzneimittel

    Dosage Form : Tablet

    Brand Name : Oxycodone/Naloxone Betaph...

    Dosage Strength : 40mg;20mg

    Packaging :

    Approval Date : 22/06/2016

    Application Number : 20141118000040

    Regulatory Info : Deregistered

    Registration Country : Sweden

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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.