Aspen API. More than just an API™

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01 2Aspen Healthcare Malta Limited
02 12Care4 Aps
03 42care4 ApS
04 4Abacus Medicine A/S
05 2MYLAN SPA
06 3Medartuum Ab
07 1Mylan Pharmaceuticals Limited
08 1Omnia L?kemedel Ab
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11 22Orifarm Ab
12 9Paranova Pharmaceuticals Ab
13 1Pharma MT
14 1Synthon Bv
15 2TEVA GMBH
16 2TEVA PHARMACEUTICALS LTD
17 2Teva GmbH
18 8Teva Gmbh
19 3Teva Pharma Ag
20 1Teva Pharmaceuticals (Uk)
21 2Teva Pharmaceuticals Limited
22 8Viatris Limited
23 2Viatris Pharma Gmbh
24 2Zentiva K.S.
25 1Zoetis Belgium Sa
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01 9Glatiramer
02 55Glatiramer Acetate
03 5Glatiramer acetate
04 5Glatirameracetat
05 4Glatiramero Acetate
06 5Glatiramerum
07 1Synthetic Peptide Analogue Of Gonadotrophin-Releasing Factor (Gnrf) Conjugated To Carrier Protein
08 2Synthetic Peptide Copolymer I
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01 1Glatiramer 20Mg 28 Joined The Parenteral Use
02 1Glatiramer 40Mg 12 Units Parenteral Use
03 4Injectable Solution In Pre-Filled Syringe
04 1Injection Solution
05 76Solution For Injection
06 3Solution For Injection In Pre-Filled
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01 6Denmark
02 4Estonia
03 6Italy
04 6Malta
05 1Moldova
06 5Norway
07 4Spain
08 49Sweden
09 5Switzerland
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01 1Brabio
02 2COPAXONE
03 1COPEMYL
04 1COPEMYLTRI
05 63Copaxone
06 1Copaxone Pen
07 5Copemyl
08 2Galtipex
09 2Glatimyl
10 2Glatiramero Viatris
11 2Glatiramyl
12 1Improvac
13 2Remurel
14 1Sclerthon
Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Galtipex
Dosage Form : Solution For Injection
Dosage Strength : 20MG
Packaging :
Approval Date : 2018-04-30
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Galtipex
Dosage Form : Solution For Injection
Dosage Strength : 40MG
Packaging :
Approval Date : 2018-04-30
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Copaxone
Dosage Form : Solution For Injection
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 11-09-2025
Application Number : 2.03E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Copaxone
Dosage Form : Solution For Injection
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 17-11-2025
Application Number : 2.03E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Copaxone
Dosage Form : Solution For Injection
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 11-09-2025
Application Number : 2.03E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Copaxone
Dosage Form : Solution For Injection
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 17-11-2025
Application Number : 2.03E+13
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Copaxone
Dosage Form : Solution For Injection
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 15-03-2017
Application Number : 2.02E+13
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Prescription
Registration Country : Denmark
Brand Name : Copaxone
Dosage Form : Solution For Injection
Dosage Strength : 40mg/ml
Packaging :
Approval Date : 31-05-2021
Application Number : 28106618821
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Copaxone
Dosage Form : Solution For Injection
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 28-09-2016
Application Number : 2.02E+13
Regulatory Info : Deregistered
Registration Country : Sweden

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.
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Copaxone
Dosage Form : Solution For Injection
Dosage Strength : 20mg/ml
Packaging :
Approval Date : 28-09-2016
Application Number : 2.02E+13
Regulatory Info : Deregistered
Registration Country : Sweden
