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01 1Aripiprazole
02 1Atomoxetine
03 1Bromocriptine
04 2Bupropion Hydrochloride
05 1Fluvoxamine Maleate
06 1Iron
07 1Klopidogrel
08 4Methylphenidate Hydrochloride
09 1Sapropterin Dihydrochloride
10 2Sumatriptan Succinate
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01 2Coated Tablet
02 2Film Coated Tablet
03 1Hard Capsule
04 2Modified Release Tablet
05 1Oral Solution
06 1Soluble Tablet
07 1Solution For Injection
08 5Tablet
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01 2100MG
02 1100mg
03 1150MG
04 118MG
05 118mg
06 11MG/ML
07 12.5MG
08 120MG/ML
09 127mg
10 1300MG
11 136mg
12 150mg
13 154mg
14 175mg
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01 8Malta
02 7Sweden
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01 1Aripiprazol Generis
02 1Atomoxetina Generis
03 1Bromocriptina Generis
04 2Bupropion Generis
05 1Clopidogrel Farma Aps
06 1Fluvoxamina Generis
07 1Iron Sucrose Generis
08 4Methylphenidate Generis
09 1Sapropterina Generis
10 2Sariptan
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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Dosage Strength : 75mg
Packaging :
Brand Name : Clopidogrel Farma Aps
Approval Date : 04/02/2011
Application Number : 20080823000016
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Dosage Strength : 18mg
Packaging :
Brand Name : Methylphenidate Generis
Approval Date : 10/02/2022
Application Number : 20190722000052
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Tablet
Dosage Strength : 27mg
Packaging :
Brand Name : Methylphenidate Generis
Approval Date : 10/02/2022
Application Number : 20190722000069
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Oral Solution
Dosage Strength : 1MG/ML
Packaging :
Brand Name : Aripiprazol Generis
Approval Date : 2023-09-19
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Hard Capsule
Dosage Strength : 18MG
Packaging :
Brand Name : Atomoxetina Generis
Approval Date : 2025-07-02
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 2.5MG
Packaging :
Brand Name : Bromocriptina Generis
Approval Date : 2020-09-10
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Modified Release Tablet
Dosage Strength : 300MG
Packaging :
Brand Name : Bupropion Generis
Approval Date : 2024-10-15
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Modified Release Tablet
Dosage Strength : 150MG
Packaging :
Brand Name : Bupropion Generis
Approval Date : 2024-10-15
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Film Coated Tablet
Dosage Strength : 100MG
Packaging :
Brand Name : Fluvoxamina Generis
Approval Date : 2018-06-12
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Solution For Injection
Dosage Strength : 20MG/ML
Packaging :
Brand Name : Iron Sucrose Generis
Approval Date : 2017-02-02
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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