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01 1Acetylsalicylic Acid
02 2Aciclovir
03 1Calcium Folinate
04 1Domperidone
05 4Ibuprofen
06 1Metoclopramide Hydrochloride
07 1Metoclopramide Hydrochloride Anhydrous
08 1Minoxidil
09 1Ranitidine
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01 1Capsule
02 1Cutaneous Solution
03 4Film Coated Tablet
04 1Oral Suspension
05 2Solution For Injection
06 4Tablet
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01 1100MG
02 210MG
03 115MG
04 11MG/ML
05 1200MG
06 120MG
07 150MG
08 1800MG
09 4Blank
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01 8Malta
02 4Moldova
03 1Spain
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01 1Asp
02 2Cicloviral
03 1Cinet
04 4IBUprim 600
05 1Medifolin
06 2Metoclopramide Medinfar
07 1Pep-Rani,
08 1Tilak
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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 100MG
Packaging :
Brand Name : Asp
Approval Date : 2014-02-13
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 200MG
Packaging :
Brand Name : Cicloviral
Approval Date : 2014-01-30
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 800MG
Packaging :
Brand Name : Cicloviral
Approval Date : 2014-01-30
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Capsule
Dosage Strength : 15MG
Packaging :
Brand Name : Medifolin
Approval Date : 2024-07-18
Application Number :
Regulatory Info : Authorised
Registration Country : Malta

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Oral Suspension
Dosage Strength : 1MG/ML
Packaging :
Brand Name : Cinet
Approval Date : 2013-11-21
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Brand Name : Metoclopramide Medinfar
Approval Date : 2014-01-14
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Film Coated Tablet
Dosage Strength :
Packaging :
Brand Name : IBUprim 600
Approval Date : 03-05-2024
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Film Coated Tablet
Dosage Strength :
Packaging :
Brand Name : IBUprim 600
Approval Date : 03-05-2024
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Film Coated Tablet
Dosage Strength :
Packaging :
Brand Name : IBUprim 600
Approval Date : 03-05-2024
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Film Coated Tablet
Dosage Strength :
Packaging :
Brand Name : IBUprim 600
Approval Date : 03-05-2024
Application Number :
Regulatory Info :
Registration Country : Moldova
