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01 6F. Hoffmann-La Roche
02 2Genentech
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01 1Dry Sub
02 2INF
03 2POWDER FOR SOLUTION
04 2POWDER;INTRAVENOUS
05 1Trockensub
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01 2Originator
02 2Prescription
03 4Blank
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01 4POLIVY
02 2Polivy
03 1Polivy 140 mg
04 1Polivy 30 mg
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01 2Canada
02 2South Africa
03 2Switzerland
04 2USA
Regulatory Info :
Registration Country : Switzerland
Brand Name : Polivy
Dosage Form : Dry Sub
Dosage Strength : 140mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Polivy
Dosage Form : Trockensub
Dosage Strength : 30mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : POLIVY
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 30MG/VIAL
Packaging :
Approval Date :
Application Number : 2515431
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : POLIVY
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 140MG/VIAL
Packaging :
Approval Date :
Application Number : 2499614
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Polivy 30 mg
Dosage Form : INF
Dosage Strength : 30mg
Packaging : 1X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Polivy 140 mg
Dosage Form : INF
Dosage Strength : 140mg
Packaging : 1X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info :
Registration Country : USA
Brand Name : POLIVY
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 140MG/VIAL
Packaging :
Approval Date :
Application Number : 761121
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : POLIVY
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 30MG/VIAL
Packaging :
Approval Date :
Application Number : 761121
Regulatory Info :
Registration Country : USA