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01 2Allopurinol
02 2Betahistine Dihydrochloride
03 1Bezafibrate
04 1Cinnarizine; Dimenhydrinate
05 5Cinnarizine; Dimenhydrinate
06 1Metformin Hydrochloride; Sitagliptin
07 3Sitagliptin
08 1Sitagliptin; Metformin Hydrochloride
09 3Tadalafil
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01 1Hennig Arzneimittel Ag
02 11Hennig Arzneimittel GmbH & Co KG
03 4Hennig Arzneimittel Gmbh & Co. Kg
04 3Hennig Arzneimittel Gmbh&Co. Kg
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01 9Film Coated Tablet
02 10Tablet
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01 11000MG; 50MG
02 2100MG
03 110MG
04 116mg
05 120MG
06 520mg; 40mg
07 120mg;40mg
08 125MG
09 1300MG
10 1400MG
11 150MG
12 150MG; 850MG
13 15MG
14 18mg
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01 1Denmark
02 1Estonia
03 11Malta
04 3Moldova
05 3Sweden
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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Tablet
Brand Name : Cellidrin
Dosage Strength : 100MG
Packaging :
Approval Date : 2006-08-30
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Tablet
Brand Name : Cellidrin
Dosage Strength : 300MG
Packaging :
Approval Date : 2006-08-30
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Vertisan
Dosage Strength : 8mg
Packaging :
Approval Date : 15-10-2015
Application Number : 2.02E+13
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Deregistered
Registration Country : Sweden
Dosage Form : Tablet
Brand Name : Vertisan
Dosage Strength : 16mg
Packaging :
Approval Date : 15-10-2015
Application Number : 2.02E+13
Regulatory Info : Deregistered
Registration Country : Sweden

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Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Film Coated Tablet
Brand Name : Befibrat
Dosage Strength : 400MG
Packaging :
Approval Date : 2006-11-01
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta

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Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Tablet
Brand Name : Arlevert
Dosage Strength : 20mg; 40mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Tablet
Brand Name : Arlevert
Dosage Strength : 20mg; 40mg
Packaging :
Approval Date : 06-05-2022
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Tablet
Brand Name : Arlevert
Dosage Strength : 20mg; 40mg
Packaging :
Approval Date : 06-05-2022
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info :
Registration Country : Moldova
Dosage Form : Tablet
Brand Name : Arlevert
Dosage Strength : 20mg; 40mg
Packaging :
Approval Date : 06-05-2022
Application Number :
Regulatory Info :
Registration Country : Moldova

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Tablet
Brand Name : Arlevert
Dosage Strength : 20mg; 40mg
Packaging :
Approval Date : 16-05-2007
Application Number : 28104050606
Regulatory Info : Prescription
Registration Country : Denmark
