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01 11CSL Behring
02 3Grifols International
03 3LFB Group
04 6Octapharma
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01 6Injection/Infusion Solution
02 5POWDER FOR SOLUTION
03 3Powder And Solvent For Injectable Solution
04 2Powder And Solvent For Injectable Solution Or Infusion
05 3Powder And Solvent For Injection Solution
06 4Solution For Injection
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01 8Approved
02 8Authorized
03 2Deregistered
04 5Schedule D
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01 3Fanhdi
02 3HUMATE-P
03 2Haemate
04 2Haemate P
05 4Voncento
06 2WILATE
07 4Wilate
08 3Willfact
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01 5Canada
02 8Spain
03 10Sweden
Regulatory Info : Approved
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Haemate
Dosage Form : Injection/Infusion Solution
Dosage Strength : 1000IUFVIII/2400IUVWF
Packaging :
Approval Date : 12/06/1987
Application Number : 19870612000136
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Haemate
Dosage Form : Injection/Infusion Solution
Dosage Strength : 500IUFVIII/1200IUVWF
Packaging :
Approval Date : 12/06/1987
Application Number : 19870612000051
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Voncento
Dosage Form : Injection/Infusion Solution
Dosage Strength : 1000IUFVIII/2400IUVWF
Packaging :
Approval Date : 12/08/2013
Application Number : 20120121000056
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Voncento
Dosage Form : Injection/Infusion Solution
Dosage Strength : 250IEFVIII/600IEVWF
Packaging :
Approval Date : 12/08/2013
Application Number : 20120121000025
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Voncento
Dosage Form : Injection/Infusion Solution
Dosage Strength : 10ml
Packaging :
Approval Date : 12/08/2013
Application Number : 20120121000032
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Voncento
Dosage Form : Injection/Infusion Solution
Dosage Strength : 5ml
Packaging :
Approval Date : 12/08/2013
Application Number : 20120121000049
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Schedule D
Registration Country : Canada
Brand Name : HUMATE-P
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 600UNIT/5ML
Packaging : 5ML
Approval Date :
Application Number : 2261219
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Brand Name : HUMATE-P
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1200UNIT/10ML
Packaging : 10ML
Approval Date :
Application Number : 2261227
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Brand Name : HUMATE-P
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2400UNIT/15ML
Packaging : 15ML
Approval Date :
Application Number : 2261235
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Authorized
Registration Country : Spain
Factor Viii; Von Willebrand Factor
Brand Name : Haemate P
Dosage Form : Powder And Solvent For Injectable Solution Or Infusion
Dosage Strength : 2400IU; 1000 IU
Packaging :
Approval Date : 1986-01-01
Application Number : 56868
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Factor Viii; Von Willebrand Factor
Brand Name : Haemate P
Dosage Form : Powder And Solvent For Injectable Solution Or Infusion
Dosage Strength : 1200IU; 500 IU
Packaging :
Approval Date : 1986-01-01
Application Number : 56867
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Factor Viii; Von Willebrand Factor
Brand Name : Fanhdi
Dosage Form : Powder And Solvent For Injection Solution
Dosage Strength : 100IU; 120IU
Packaging :
Approval Date : 1994-12-01
Application Number : 60602
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Factor Viii; Von Willebrand Factor
Brand Name : Fanhdi
Dosage Form : Powder And Solvent For Injection Solution
Dosage Strength : 50IU; 60IU
Packaging :
Approval Date : 1994-12-01
Application Number : 60600
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Factor Viii; Von Willebrand Factor
Brand Name : Fanhdi
Dosage Form : Powder And Solvent For Injection Solution
Dosage Strength : 25IU; 30 IU
Packaging :
Approval Date : 1994-12-01
Application Number : 60601
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Approved
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Wilate
Dosage Form : Solution For Injection
Dosage Strength : 1000IEVWF/1000IEFVIII
Packaging :
Approval Date : 02/08/2012
Application Number : 20101127000080
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Wilate
Dosage Form : Solution For Injection
Dosage Strength : 500IEVWF/500IEFVIII
Packaging :
Approval Date : 02/08/2012
Application Number : 20101127000073
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Wilate
Dosage Form : Solution For Injection
Dosage Strength : 450IEFVIII/400IEVWF
Packaging :
Approval Date : 31/08/2007
Application Number : 20060826000015
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Coagulation Factor VIII Human; Von Willebrand Factor Human
Brand Name : Wilate
Dosage Form : Solution For Injection
Dosage Strength : 900IEFVIII/800IEVWF
Packaging :
Approval Date : 31/08/2007
Application Number : 20060826000022
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Schedule D
Registration Country : Canada
Brand Name : WILATE
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500UNIT/5ML
Packaging : 5ML
Approval Date :
Application Number : 2286750
Regulatory Info : Schedule D
Registration Country : Canada
Regulatory Info : Schedule D
Registration Country : Canada
Brand Name : WILATE
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1000UNIT/10ML
Packaging : 10ML
Approval Date :
Application Number : 2286769
Regulatory Info : Schedule D
Registration Country : Canada