Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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01 4Sanofi
02 2Octapharma
03 20Swedish Orphan Biovitrum AB
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01 2INJ
02 1Injectable Solution
03 2KIT
04 2POWDER FOR SOLUTION
05 5Powder And Solvent For Injectable Solution
06 14Solution For Injection
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01 5Allowed
02 5Approved
03 5Authorized
04 5Marketed
05 2Originator
06 4Schedule D
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01 4ALPROLIX
02 18Alprolix
03 2Alprolix IE
04 2Octaplex 500 IU
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01 4Canada
02 5Norway
03 2South Africa
04 5Spain
05 5Sweden
06 5Switzerland
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Schedule D
Registration Country : Canada
RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN
Brand Name : ALPROLIX
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500UNIT/VIAL
Packaging :
Approval Date :
Application Number : 2422913
Regulatory Info : Schedule D
Registration Country : Canada
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Schedule D
Registration Country : Canada
RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN
Brand Name : ALPROLIX
Dosage Form : KIT
Dosage Strength : 1000UNIT/VIAL
Packaging :
Approval Date :
Application Number : 2422921
Regulatory Info : Schedule D
Registration Country : Canada
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Schedule D
Registration Country : Canada
RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN
Brand Name : ALPROLIX
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2000UNIT/VIAL
Packaging :
Approval Date :
Application Number : 2422948
Regulatory Info : Schedule D
Registration Country : Canada
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Schedule D
Registration Country : Canada
RECOMBINANT HUMAN COAGULATION FACTOR IX, FC FUSION PROTEIN
Brand Name : ALPROLIX
Dosage Form : KIT
Dosage Strength : 3000UNIT/VIAL
Packaging :
Approval Date :
Application Number : 2422956
Regulatory Info : Schedule D
Registration Country : Canada
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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 250IU/5ml
Packaging :
Approval Date : 25/10/2016
Application Number : 66039
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 500IU/5ml
Packaging :
Approval Date : 25/10/2016
Application Number : 66039
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 1000IU/5ml
Packaging :
Approval Date : 25/10/2016
Application Number : 66039
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Alprolix IE
Dosage Form : Solution For Injection
Dosage Strength : 2000IU/5ml
Packaging :
Approval Date : 25/10/2016
Application Number : 66039
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Alprolix IE
Dosage Form : Injectable Solution
Dosage Strength : 3000IU/5ml
Packaging :
Approval Date : 25/10/2016
Application Number : 66039
Regulatory Info : Allowed
Registration Country : Switzerland

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Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 1000IU
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 2000IU
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 250IU
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 3000IU
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Marketed
Registration Country : Norway
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 500IU
Packaging :
Approval Date :
Application Number :
Regulatory Info : Marketed
Registration Country : Norway

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Alprolix
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 500IU
Packaging :
Approval Date : 23-06-2016
Application Number : 1161098002
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Alprolix
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 1000IU
Packaging :
Approval Date : 23-06-2016
Application Number : 1161098003
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Alprolix
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 250IU
Packaging :
Approval Date : 22-06-2016
Application Number : 1161098001
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Alprolix
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 2000IU
Packaging :
Approval Date : 23-06-2016
Application Number : 1161098004
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Alprolix
Dosage Form : Powder And Solvent For Injectable Solution
Dosage Strength : 3000IU
Packaging :
Approval Date : 23-06-2016
Application Number : 1161098005
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Alprolix
Dosage Form : Solution For Injection
Dosage Strength : 250IE
Packaging :
Approval Date : 12-05-2016
Application Number : 2.02E+13
Regulatory Info : Approved
Registration Country : Sweden
