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01 2Ambrisentan
02 1Anagrelide Hydrochloride Monohydrate
03 1Naltrexone Hydrochloride
04 1Naltrexonhydroklorid
05 4Ropeginterferon Alfa-2B
06 1Ropeginterferon alfa-2b
07 2Sugammadex Sodium
08 1Tadalafil
09 1Tetrabenazin
10 1Tetrabenazine
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01 1AOP Orphan Pharmaceuticals AG
02 14Aop Orphan Pharmaceuticals Gmbh
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01 1Capsule
02 5Film Coated Tablet
03 1Injectable Solution
04 1Injection Solution
05 5Solution For Injection
06 2Tablet
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01 10.5mg
02 2100mg/ml
03 110mg
04 120mg
05 3250mcg/0.5ml
06 225mg
07 2500mcg/0.5ml
08 250mg
09 15mg
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01 5Denmark
02 1Norway
03 9Sweden
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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Ambrisentan Aop
Dosage Strength : 10mg
Packaging :
Approval Date : 13/01/2021
Application Number : 20190328000081
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Ambrisentan Aop
Dosage Strength : 5mg
Packaging :
Approval Date : 13/01/2021
Application Number : 20190328000074
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Anagrelide Hydrochloride Monohydrate
Dosage Form : Capsule
Brand Name : Anagrelide Aop
Dosage Strength : 0.5mg
Packaging :
Approval Date : 08/05/2018
Application Number : 20161201000085
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Film Coated Tablet
Brand Name : Naltrexon \"Aop\"
Dosage Strength : 50mg
Packaging :
Approval Date : 15-09-2005
Application Number : 28103785105
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Brand Name : Naltrexon Vitaflo
Dosage Strength : 50mg
Packaging :
Approval Date : 04/02/2005
Application Number : 20040607008829
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Besremi
Dosage Strength : 250mcg/0.5ml
Packaging :
Approval Date : 15/02/2019
Application Number : 20170208000073
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Solution For Injection
Brand Name : Besremi
Dosage Strength : 500mcg/0.5ml
Packaging :
Approval Date : 15/02/2019
Application Number : 20170208000080
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Marketed
Registration Country : Norway
Dosage Form : Solution For Injection
Brand Name : Besremi
Dosage Strength : 250mcg/0.5ml
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Solution For Injection
Brand Name : Besremi
Dosage Strength : 250mcg/0.5ml
Packaging :
Approval Date : 15-02-2019
Application Number : 28105912117
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Solution For Injection
Brand Name : Besremi
Dosage Strength : 500mcg/0.5ml
Packaging :
Approval Date : 15-02-2019
Application Number : 28105912217
Regulatory Info : Prescription
Registration Country : Denmark
