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PharmaCompass

01

BePharma
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LAZERTINIB MESYLATE

Brand Name : LAZCLUZE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 80MG BASE

Packaging :

Approval Date : 2024-08-19

Application Number : 219008

Regulatory Info : RX

Registration Country : USA

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02

BePharma
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BePharma
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LAZERTINIB MESYLATE

Brand Name : LAZCLUZE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 240MG BASE

Packaging :

Approval Date : 2024-08-19

Application Number : 219008

Regulatory Info : RX

Registration Country : USA

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03

BePharma
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LAZERTINIB (LAZERTINIB MESYLATE)

Brand Name : LAZCLUZE

Dosage Form : TABLET

Dosage Strength : 80MG

Packaging :

Approval Date :

Application Number : 2555964

Regulatory Info : Prescription

Registration Country : Canada

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04

BePharma
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BePharma
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LAZERTINIB (LAZERTINIB MESYLATE)

Brand Name : LAZCLUZE

Dosage Form : TABLET

Dosage Strength : 240MG

Packaging :

Approval Date :

Application Number : 2555972

Regulatory Info : Prescription

Registration Country : Canada

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05

BePharma
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Lazertinib

Brand Name : Lazcluze

Dosage Form : Film-Coated Tablet

Dosage Strength : 240mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Estonia

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06

BePharma
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BePharma
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Lazertinib

Brand Name : Lazcluze

Dosage Form : Film-Coated Tablet

Dosage Strength : 80mg

Packaging :

Approval Date :

Application Number :

Regulatory Info : Prescription

Registration Country : Estonia

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07

BePharma
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BePharma
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Lazertinib

Brand Name : Lazcluze

Dosage Form : Film Coated Tablet

Dosage Strength : 80MG

Packaging :

Approval Date : 29-01-2025

Application Number : 1241886001

Regulatory Info : Authorized

Registration Country : Spain

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08

BePharma
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BePharma
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Lazertinib

Brand Name : Lazcluze

Dosage Form : Film Coated Tablet

Dosage Strength : 240MG

Packaging :

Approval Date : 29-01-2025

Application Number : 1241886005

Regulatory Info : Authorized

Registration Country : Spain

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09

BePharma
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BePharma
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Lazertinib

Brand Name : Lazcluze

Dosage Form : Film Coated Tablet

Dosage Strength : 240mg

Packaging :

Approval Date : 20-01-2025

Application Number : 28107094023

Regulatory Info : Prescription

Registration Country : Denmark

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10

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BePharma
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Lazertinib

Brand Name : Lazcluze

Dosage Form : Film Coated Tablet

Dosage Strength : 80mg

Packaging :

Approval Date : 20-01-2025

Application Number : 28107093923

Regulatory Info : Prescription

Registration Country : Denmark

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