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01 1GlaxoSmithKline Trading Services Limited

02 4Glaxosmithkline (Ireland) Limited

03 1Glaxosmithkline (Ireland)Limited

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PharmaCompass

01

BioProcess International US West
Not Confirmed
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BioProcess International US West
Not Confirmed

Dostarlimab

Brand Name : Jemperli

Dosage Form : Concentrate For Solution For Infusion

Dosage Strength : 500mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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02

BioProcess International US West
Not Confirmed
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BioProcess International US West
Not Confirmed

Dostarlimab

Brand Name : Jemperli

Dosage Form : Concentrate For Solution For Infusion

Dosage Strength : 500mg/10ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Estonia

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03

BioProcess International US West
Not Confirmed
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BioProcess International US West
Not Confirmed

Dostarlimab

Brand Name : Jemperli

Dosage Form : Concentrate For Infusion Solution

Dosage Strength : 500MG

Packaging :

Approval Date : 25-05-2021

Application Number : 1211538001

Regulatory Info : Authorized

Registration Country : Spain

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04

BioProcess International US West
Not Confirmed
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BioProcess International US West
Not Confirmed

Dostarlimab

Brand Name : Jemperli

Dosage Form : Concentrate For Solution For Infusion

Dosage Strength : 500MG

Packaging :

Approval Date : 08-08-2025

Application Number : 1211538001IP

Regulatory Info : Authorized

Registration Country : Spain

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05

BioProcess International US West
Not Confirmed
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BioProcess International US West
Not Confirmed

Dostarlimab

Brand Name : Jemperli

Dosage Form : Concentrate For Solution For Infusion

Dosage Strength : 500mg

Packaging :

Approval Date : 21-04-2021

Application Number : 28106416220

Regulatory Info : Prescription

Registration Country : Denmark

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06

BioProcess International US West
Not Confirmed
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BioProcess International US West
Not Confirmed

Dostarlimab

Brand Name : Jemperli

Dosage Form : Concentrate For Solution For Infusion

Dosage Strength : 500mg

Packaging :

Approval Date : 21-04-2021

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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