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01 8Novo Nordisk
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01 4POWDER FOR SOLUTION
02 4Trockensub
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01 8Blank
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01 4REBINYN
02 4Refixia
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01 4Canada
02 4Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Refixia
Dosage Form : Trockensub
Dosage Strength : 1000iu
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Refixia
Dosage Form : Trockensub
Dosage Strength : 2000iu
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Refixia
Dosage Form : Trockensub
Dosage Strength : 500iu
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Refixia
Dosage Form : Trockensub
Dosage Strength : 3000iu
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Canada
COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
Brand Name : REBINYN
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 500UNIT/VIAL
Packaging : 500 IU VIAL
Approval Date :
Application Number : 2470187
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
Brand Name : REBINYN
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 3000UNIT/VIAL
Packaging :
Approval Date :
Application Number : 2532964
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
Brand Name : REBINYN
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 1000UNIT/VIAL
Packaging : 1000 IU VIAL
Approval Date :
Application Number : 2470268
Regulatory Info :
Registration Country : Canada
Regulatory Info :
Registration Country : Canada
COAGULATION FACTOR IX (RECOMBINANT), PEGYLATED
Brand Name : REBINYN
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 2000UNIT/VIAL
Packaging : 2000 IU VIAL
Approval Date :
Application Number : 2470276
Regulatory Info :
Registration Country : Canada