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01 17GSK

02 1GlaxoSmithKline Trading

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PharmaCompass

01

VMX
Not Confirmed
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VMX
Not Confirmed

MEPOLIZUMAB

Brand Name : NUCALA

Dosage Form : INJECTABLE;SUBCUTANEOUS LYOPHILIZED POWER

Dosage Strength : 100MG

Packaging :

Approval Date :

Application Number : 125526

Regulatory Info :

Registration Country : USA

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02

VMX
Not Confirmed
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VMX
Not Confirmed

MEPOLIZUMAB

Brand Name : NUCALA

Dosage Form : INJECTABLE;SUBCUTANEOUS

Dosage Strength : 100MG/ML

Packaging :

Approval Date :

Application Number : 761122

Regulatory Info :

Registration Country : USA

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03

VMX
Not Confirmed
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VMX
Not Confirmed

Mepolizumabum

Brand Name : Nucala

Dosage Form : Dry Sub

Dosage Strength : 100mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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04

VMX
Not Confirmed
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VMX
Not Confirmed

Mepolizumabum

Brand Name : Nucala

Dosage Form : Inj L?s

Dosage Strength : 100mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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05

VMX
Not Confirmed
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VMX
Not Confirmed

Mepolizumabum

Brand Name : Nucala

Dosage Form : Inj L?s

Dosage Strength : 100mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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06

VMX
Not Confirmed
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VMX
Not Confirmed

Mepolizumabum

Brand Name : Nucala

Dosage Form : Inj L?s

Dosage Strength : 100mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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07

VMX
Not Confirmed
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VMX
Not Confirmed

MEPOLIZUMAB

Brand Name : NUCALA

Dosage Form : SOLUTION

Dosage Strength : 100MG/ML

Packaging :

Approval Date :

Application Number : 2492989

Regulatory Info :

Registration Country : Canada

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08

VMX
Not Confirmed
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VMX
Not Confirmed

MEPOLIZUMAB

Brand Name : NUCALA

Dosage Form : SOLUTION

Dosage Strength : 100MG/ML

Packaging :

Approval Date :

Application Number : 2492997

Regulatory Info :

Registration Country : Canada

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09

VMX
Not Confirmed
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VMX
Not Confirmed

MEPOLIZUMAB

Brand Name : NUCALA

Dosage Form : SOLUTION

Dosage Strength : 40MG/0.4ML

Packaging :

Approval Date :

Application Number : 2530821

Regulatory Info :

Registration Country : Canada

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10

VMX
Not Confirmed
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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11

VMX
Not Confirmed
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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12

VMX
Not Confirmed
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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13

VMX
Not Confirmed
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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14

VMX
Not Confirmed
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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15

VMX
Not Confirmed
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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16

VMX
Not Confirmed
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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17

VMX
Not Confirmed
arrow
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form :

Dosage Strength :

Packaging : 1

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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18

GlaxoSmithKline Trading

Country
VMX
Not Confirmed
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GlaxoSmithKline Trading

Country
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VMX
Not Confirmed

mepolizumab

Brand Name : Nucala

Dosage Form : POWDER FOR SOLUTION FOR INJECTION

Dosage Strength : 100 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

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