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01 1Amiodarone Hydrochloride
02 2Ebastine
03 2Enalapril Maleate
04 1Fluoxetine Hydrochloride
05 2Solifenacin Succinate
06 1Sulpiride
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01 2Film Coated Tablet
02 1Hard Capsule
03 2Orodispersible Tablet
04 4Tablet
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01 210mg
02 2200MG
03 120MG
04 120mg
05 122.5MG
06 15MG
07 15mg
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01 5Malta
02 4Sweden
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01 1Amiodarone
02 2Ebastine Medreich
03 2Enalapril
04 1Fluoxetine
05 2Solifenacin Medreich
06 1Sulpiride
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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Orodispersible Tablet
Dosage Strength : 10mg
Packaging :
Brand Name : Ebastine Medreich
Approval Date : 23/05/2018
Application Number : 20161201000207
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Orodispersible Tablet
Dosage Strength : 20mg
Packaging :
Brand Name : Ebastine Medreich
Approval Date : 23/05/2018
Application Number : 20161201000214
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Dosage Strength : 10mg
Packaging :
Brand Name : Solifenacin Medreich
Approval Date : 22/11/2017
Application Number : 20160430000156
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Film Coated Tablet
Dosage Strength : 5mg
Packaging :
Brand Name : Solifenacin Medreich
Approval Date : 22/11/2017
Application Number : 20160430000149
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Invalid
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 200MG
Packaging :
Brand Name : Amiodarone
Approval Date : 2013-09-13
Application Number :
Regulatory Info : Invalid
Registration Country : Malta

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Regulatory Info : Invalid
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Brand Name : Enalapril
Approval Date : 2013-05-30
Application Number :
Regulatory Info : Invalid
Registration Country : Malta

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Regulatory Info : Invalid
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 20MG
Packaging :
Brand Name : Enalapril
Approval Date : 2013-05-31
Application Number :
Regulatory Info : Invalid
Registration Country : Malta

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Regulatory Info : Invalid
Registration Country : Malta
Dosage Form : Hard Capsule
Dosage Strength : 22.5MG
Packaging :
Brand Name : Fluoxetine
Approval Date : 2017-02-14
Application Number :
Regulatory Info : Invalid
Registration Country : Malta

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Regulatory Info : Invalid
Registration Country : Malta
Dosage Form : Tablet
Dosage Strength : 200MG
Packaging :
Brand Name : Sulpiride
Approval Date : 2013-05-27
Application Number :
Regulatory Info : Invalid
Registration Country : Malta

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