Synopsis
Synopsis
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NDC API
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Molecular Weight | 763.0 g/mol |
---|---|
Molecular Formula | C42H66O12 |
XLogP3 | 5.1 |
Hydrogen Bond Donor Count | 7 |
Hydrogen Bond Acceptor Count | 12 |
Rotatable Bond Count | 6 |
Exact Mass | 762.45542754 g/mol |
Monoisotopic Mass | 762.45542754 g/mol |
Topological Polar Surface Area | 203 Ų |
Heavy Atom Count | 54 |
Formal Charge | 0 |
Complexity | 1530 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 15 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Shanghai Minbiotech is the leading producer of biopharmaceuticals and a variety of high-end generic & innovative drugs.
About the Company : Headquartered in Fengxian District, Shanghai Minbiotech Co., Ltd. is a company specializing in the R&D and production of advanced pharmaceutical intermediates and biological API...
About the Company : Beijing Mesochem Technology Co. Ltd., which is located in the national economic and technological development area of Yizhuang, China, manufactures pharmaceutical chemicals, fine c...
Regulatory Info :
Registration Country : USA
Brand Name : NUCALA
Dosage Form : INJECTABLE;SUBCUTANEOUS LYOPHILIZED POWER
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number : 125526
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : Switzerland
Brand Name : Nucala
Dosage Form : Inj L?s
Dosage Strength : 100mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info :
Registration Country : Switzerland
Brand Name : Nucala
Dosage Form : Inj L?s
Dosage Strength : 100mg/ml
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : NUCALA
Dosage Form : SOLUTION
Dosage Strength : 100MG/ML
Packaging :
Approval Date :
Application Number : 2492989
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : NUCALA
Dosage Form : SOLUTION
Dosage Strength : 40MG/0.4ML
Packaging :
Approval Date :
Application Number : 2530821
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info :
Registration Country : Australia
Brand Name : Nucala
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Nucala
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Nucala
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Nucala
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Regulatory Info :
Registration Country : Australia
Brand Name : Nucala
Dosage Form :
Dosage Strength :
Packaging : 1
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
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PharmaCompass offers a list of Mepolizumab API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Mepolizumab manufacturer or Mepolizumab supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mepolizumab manufacturer or Mepolizumab supplier.
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A Mepolizumab manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mepolizumab, including repackagers and relabelers. The FDA regulates Mepolizumab manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mepolizumab API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Mepolizumab manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mepolizumab supplier is an individual or a company that provides Mepolizumab active pharmaceutical ingredient (API) or Mepolizumab finished formulations upon request. The Mepolizumab suppliers may include Mepolizumab API manufacturers, exporters, distributors and traders.
click here to find a list of Mepolizumab suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Mepolizumab Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Mepolizumab GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Mepolizumab GMP manufacturer or Mepolizumab GMP API supplier for your needs.
A Mepolizumab CoA (Certificate of Analysis) is a formal document that attests to Mepolizumab's compliance with Mepolizumab specifications and serves as a tool for batch-level quality control.
Mepolizumab CoA mostly includes findings from lab analyses of a specific batch. For each Mepolizumab CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Mepolizumab may be tested according to a variety of international standards, such as European Pharmacopoeia (Mepolizumab EP), Mepolizumab JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Mepolizumab USP).