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01 1Ethypharm Sa

02 1Aguettant Laboratory

03 1Laboratoire Aguettant

04 1PANPHARMA

05 1Panpharma Sa

06 1Viatris Ab

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEthypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.

Regulatory Info : Approved

Registration Country : Sweden

Suxamethonium Chloride (Dihydrate)

Brand Name : Suxamethonium Ethypharm

Dosage Form : Solution For Injection/Infusion

Dosage Strength : 50mg/ml

Packaging :

Approval Date : 05-04-2019

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

Ethypharm

02

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

Suksametoniumkloriddihydrat

Brand Name : Suxamethonium chloride Aguettant

Dosage Form : Solution For Injection

Dosage Strength : 10mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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03

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

Suxamethonium Chloride Dihydrate

Brand Name : Zennux

Dosage Form : Injectable Solution In Pre-Filled Syringe

Dosage Strength : 10MG

Packaging :

Approval Date : 09-10-2020

Application Number : 85344

Regulatory Info : Authorized

Registration Country : Spain

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04

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

Suksametoniumkloriddihydrat

Brand Name : Suxamethonium chloride Panpharma

Dosage Form : Solution For Injection/Infusion

Dosage Strength : 50mg/ml

Packaging :

Approval Date :

Application Number :

Regulatory Info : Marketed

Registration Country : Norway

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05

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

Suxamethonium Chloride (Dihydrate)

Brand Name : Suxamethonium Chloride Panpharma

Dosage Form : Solution For Injection/Infusion

Dosage Strength : 50mg/ml

Packaging :

Approval Date : 18-09-2023

Application Number : 2.02E+13

Regulatory Info : Approved

Registration Country : Sweden

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06

BioAsia
Not Confirmed
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BioAsia
Not Confirmed

Suxamethonium Chloride (Dihydrate)

Brand Name : Celocurin

Dosage Form : Injectable Solution

Dosage Strength : 50mg/ml

Packaging :

Approval Date : 17-12-1957

Application Number : 1.96E+13

Regulatory Info : Approved

Registration Country : Sweden

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