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01 1GIVOSIRAN (GIVOSIRAN SODIUM)
02 1GIVOSIRAN SODIUM
03 1Givosiran
04 1Givosiran Sodium
05 1LUMASIRAN (LUMASIRAN SODIUM)
06 1LUMASIRAN SODIUM
07 2Lumasiran Sodium
08 1PATISIRAN (PATISIRAN SODIUM)
09 1PATISIRAN SODIUM
10 2Patisiran Sodium
11 1VUTRISIRAN (VUTRISIRAN SODIUM)
12 1VUTRISIRAN SODIUM
13 1Vutrisiran
14 1Vutrisiran Sodium
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01 4ALNYLAM NETHERLANDS B.V.
02 4ALNYLAM PHARMS INC
03 8Alnylam Netherlands Bv
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01 1Concentrate For Infusion Solution
02 1Concentrate For Solution For Infusion
03 4Injectable Solution
04 1Injectable Solution In Pre-Filled Syringe
05 4SOLUTION
06 1SOLUTION;INTRAVENOUS
07 3SOLUTION;SUBCUTANEOUS
08 1Solution For Injection
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01 1189MG
02 1189MG/ML
03 1189mg/ml
04 125MG
05 125MG/0.5ML
06 125mg
07 12MG
08 12MG/ML
09 12mg/ml
10 194.5MG
11 194.5MG/0.5ML
12 194.5mg/0.5ml
13 1EQ 10MG BASE/5ML (EQ 2MG BASE/ML)
14 1EQ 189MG BASE/ML (EQ 189MG BASE/ML)
15 1EQ 25MG BASE/0.5ML (EQ 25MG BASE/0.5ML)
16 1EQ 94.5MG BASE/0.5ML (EQ 94.5MG BASE/0.5ML)
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01 4Canada
02 4Spain
03 4Sweden
04 4USA
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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Injectable Solution
Brand Name : Givlaari
Dosage Strength : 189MG
Packaging :
Approval Date : 2020-04-28
Application Number : 1201428001
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : GIVLAARI
Dosage Strength : 189MG/ML
Packaging :
Approval Date :
Application Number : 2506343
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : GIVLAARI
Dosage Strength : EQ 189MG BASE/ML (EQ 1...
Packaging :
Approval Date : 2019-11-20
Application Number : 212194
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Injectable Solution
Brand Name : Givlaari
Dosage Strength : 189mg/ml
Packaging :
Approval Date : 02/03/2020
Application Number : 20190702000072
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : OXLUMO
Dosage Strength : 94.5MG/0.5ML
Packaging :
Approval Date :
Application Number : 2525755
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;SUBCUTANEOUS
Brand Name : OXLUMO
Dosage Strength : EQ 94.5MG BASE/0.5ML (...
Packaging :
Approval Date : 2020-11-23
Application Number : 214103
Regulatory Info : RX
Registration Country : USA

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Regulatory Info : Approved
Registration Country : Sweden
Dosage Form : Injectable Solution
Brand Name : Oxlumo
Dosage Strength : 94.5mg/0.5ml
Packaging :
Approval Date : 19/11/2020
Application Number : 20200402000033
Regulatory Info : Approved
Registration Country : Sweden

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Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Injectable Solution
Brand Name : Oxlumo
Dosage Strength : 94.5MG
Packaging :
Approval Date : 2020-12-30
Application Number : 1201496001
Regulatory Info : Authorized
Registration Country : Spain

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Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Brand Name : ONPATTRO
Dosage Strength : 2MG/ML
Packaging :
Approval Date :
Application Number : 2489252
Regulatory Info : Prescription
Registration Country : Canada

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Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INTRAVENOUS
Brand Name : ONPATTRO
Dosage Strength : EQ 10MG BASE/5ML (EQ 2...
Packaging :
Approval Date : 2018-08-10
Application Number : 210922
Regulatory Info : RX
Registration Country : USA

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