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01 1Sanofi

02 1Accord healthcare

03 6Bayer AG

04 1Bluefish Pharmaceuticals AB

05 1Eurolab

06 1STADA Arzneimittel

07 1Sandoz B2B

08 1Teva Pharmaceutical Industries

09 1Viatris

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Allowed

Registration Country : Switzerland

Sorafenib

Brand Name : Sorafenib Zentiva

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 07/01/2021

Application Number : 68210

Regulatory Info : Allowed

Registration Country : Switzerland

Sanofi Company Banner

02

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib Tosylate

Brand Name : Sorafenib Accord

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 09/11/2022

Application Number : 20210629000013

Regulatory Info : Approved

Registration Country : Sweden

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03

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib

Brand Name : Nexavar

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 28/03/2006

Application Number : 57583

Regulatory Info : Allowed

Registration Country : Switzerland

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04

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib Tosylate

Brand Name : Nexavar

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 19/07/2006

Application Number : 20050915000019

Regulatory Info : Approved

Registration Country : Sweden

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05

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib

Brand Name : Nexavar

Dosage Form : TAB

Dosage Strength : 200mg

Packaging : 60X1mg

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

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06

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib

Brand Name : Nexavar

Dosage Form : tablet

Dosage Strength : 200 mg

Packaging : 60

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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07

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib

Brand Name : Nexavar

Dosage Form : tablet

Dosage Strength : 200 mg

Packaging : 60

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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08

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib

Brand Name : Nexavar

Dosage Form : tablet

Dosage Strength : 200 mg

Packaging : 60

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Australia

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09

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib Tosylate

Brand Name : Sorafenib Bluefish

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 24/08/2022

Application Number : 20210301000010

Regulatory Info : Approved

Registration Country : Sweden

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10

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib

Brand Name : Eurostib

Dosage Form : TAB

Dosage Strength : 200mg

Packaging : 60X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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11

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib Tosylate

Brand Name : Sorafenib Sandoz

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 14/07/2020

Application Number : 20190503000028

Regulatory Info : Approved

Registration Country : Sweden

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12

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib Tosylate

Brand Name : Sorafenib Stada

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 14/07/2020

Application Number : 20190425000045

Regulatory Info : Approved

Registration Country : Sweden

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13

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib Tosylate

Brand Name : Sorafenib Teva

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 11/01/2019

Application Number : 20171116000032

Regulatory Info : Approved

Registration Country : Sweden

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14

Luxepack
Not Confirmed
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Luxepack
Not Confirmed

Sorafenib Tosylate

Brand Name : Sorafenib Viatris

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 30/12/2020

Application Number : 20200804000037

Regulatory Info : Approved

Registration Country : Sweden

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