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01 1Aripiprazole
02 1Atomoxetine
03 1Bromocriptine
04 2Bupropion Hydrochloride
05 1Fluvoxamine Maleate
06 1Iron
07 1Sapropterin Dihydrochloride
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01 1Film Coated Tablet
02 1Hard Capsule
03 2Modified Release Tablet
04 1Oral Solution
05 1Soluble Tablet
06 1Solution For Injection
07 1Tablet
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01 2100MG
02 1150MG
03 118MG
04 11MG/ML
05 12.5MG
06 120MG/ML
07 1300MG
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01 8Malta
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01 1Aripiprazol Generis
02 1Atomoxetina Generis
03 1Bromocriptina Generis
04 2Bupropion Generis
05 1Fluvoxamina Generis
06 1Iron Sucrose Generis
07 1Sapropterina Generis
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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Regulatory Info : Withdrawn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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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Soluble Tablet
Dosage Strength : 100MG
Packaging :
Brand Name : Sapropterina Generis
Approval Date : 2025-02-12
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
