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01 3ALISKIREN HEMIFUMARATE
02 4ALISKIREN HEMIFUMARATE; HYDROCHLOROTHIAZIDE
03 2Aliskiren
04 2Aliskiren Fumarate
05 4Aliskiren Fumarate; Hydrochlorothiazide
06 2Aliskiren Hemifumarate
07 4Aliskiren Hemifumarate and Hydrochlorothiazide
08 2Aliskiren hemifumarate
09 8Aliskireno
10 4Hydrochlorothiazide; Aliskirene
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01 7NODEN PHARMA
02 14Noden Pharma Designated Activity Company
03 2The Pharma DAC node
04 12The Pharma Dac Node
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01 1CAPSULE, PELLET;ORAL
02 26Film Coated Tablet
03 2Film-Coated Tablet
04 6TABLET;ORAL
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01 4150MG
02 1150MG; 12.5 MG
03 1150MG; 25 MG
04 1150mcg; 25mg
05 4150mg
06 1150mg; 12.5mg
07 1150mg;12.5mg
08 1150mg;25mg
09 4300MG
10 1300MG; 12.5 MG
11 1300MG; 25 MG
12 4300mg
13 1300mg; 12.5mg
14 1300mg; 25mg
15 1300mg;12.5mg
16 1300mg;25mg
17 1EQ 150MG BASE
18 1EQ 150MG BASE;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
19 1EQ 150MG BASE;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
20 1EQ 300MG BASE
21 1EQ 300MG BASE;12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
22 1EQ 300MG BASE;25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
23 1EQ 37.5MG BASE
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01 6Denmark
02 2Estonia
03 2Norway
04 12Spain
05 6Sweden
06 7USA
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Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Film-Coated Tablet
Brand Name : Rasilez
Dosage Strength : 150mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Prescription
Registration Country : Estonia
Dosage Form : Film-Coated Tablet
Brand Name : Rasilez
Dosage Strength : 300mg
Packaging :
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Estonia

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Film Coated Tablet
Brand Name : Rasilez
Dosage Strength : 150mg
Packaging :
Approval Date : 22-08-2007
Application Number : 28104015806
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Dosage Form : Film Coated Tablet
Brand Name : Rasilez
Dosage Strength : 300mg
Packaging :
Approval Date : 22-08-2007
Application Number : 28104015906
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Aliskiren Fumarate; Hydrochlorothiazide
Dosage Form : Film Coated Tablet
Brand Name : Rasilez Hct
Dosage Strength : 150mg; 12.5mg
Packaging :
Approval Date : 16-01-2009
Application Number : 28104274107
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Aliskiren Fumarate; Hydrochlorothiazide
Dosage Form : Film Coated Tablet
Brand Name : Rasilez Hct
Dosage Strength : 150mcg; 25mg
Packaging :
Approval Date : 16-01-2009
Application Number : 28104274207
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Aliskiren Fumarate; Hydrochlorothiazide
Dosage Form : Film Coated Tablet
Brand Name : Rasilez Hct
Dosage Strength : 300mg; 12.5mg
Packaging :
Approval Date : 16-01-2009
Application Number : 28104274307
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : Prescription
Registration Country : Denmark
Aliskiren Fumarate; Hydrochlorothiazide
Dosage Form : Film Coated Tablet
Brand Name : Rasilez Hct
Dosage Strength : 300mg; 25mg
Packaging :
Approval Date : 16-01-2009
Application Number : 28104274407
Regulatory Info : Prescription
Registration Country : Denmark

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : TEKTURNA
Dosage Strength : EQ 150MG BASE
Packaging :
Approval Date : 2007-03-05
Application Number : 21985
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : TEKTURNA
Dosage Strength : EQ 300MG BASE
Packaging :
Approval Date : 2007-03-05
Application Number : 21985
Regulatory Info : RX
Registration Country : USA
