Synopsis
Synopsis
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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Others
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Annual Reports
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Regulatory FDF Prices
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API
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FDF
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
Molecular Weight | 902.9 g/mol |
---|---|
Molecular Formula | C39H66O23 |
XLogP3 | -3.9 |
Hydrogen Bond Donor Count | 11 |
Hydrogen Bond Acceptor Count | 23 |
Rotatable Bond Count | 23 |
Exact Mass | 902.39948835 g/mol |
Monoisotopic Mass | 902.39948835 g/mol |
Topological Polar Surface Area | 349 Ų |
Heavy Atom Count | 62 |
Formal Charge | 0 |
Complexity | 1380 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 21 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
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ABOUT THIS PAGE
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PharmaCompass offers a list of SODIUM STARCH GLYOLATE 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 SODIUM STARCH GLYOLATE manufacturer or SODIUM STARCH GLYOLATE supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred SODIUM STARCH GLYOLATE manufacturer or SODIUM STARCH GLYOLATE supplier.
PharmaCompass also assists you with knowing the SODIUM STARCH GLYOLATE API Price utilized in the formulation of products. SODIUM STARCH GLYOLATE API Price is not always fixed or binding as the SODIUM STARCH GLYOLATE Price is obtained through a variety of data sources. The SODIUM STARCH GLYOLATE Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sodium starch octenylsuccinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium starch octenylsuccinate, including repackagers and relabelers. The FDA regulates Sodium starch octenylsuccinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium starch octenylsuccinate 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 Sodium starch octenylsuccinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium starch octenylsuccinate supplier is an individual or a company that provides Sodium starch octenylsuccinate active pharmaceutical ingredient (API) or Sodium starch octenylsuccinate finished formulations upon request. The Sodium starch octenylsuccinate suppliers may include Sodium starch octenylsuccinate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium starch octenylsuccinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium starch octenylsuccinate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium starch octenylsuccinate active pharmaceutical ingredient (API) in detail. Different forms of Sodium starch octenylsuccinate DMFs exist exist since differing nations have different regulations, such as Sodium starch octenylsuccinate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium starch octenylsuccinate DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium starch octenylsuccinate USDMF includes data on Sodium starch octenylsuccinate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium starch octenylsuccinate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium starch octenylsuccinate suppliers with USDMF on PharmaCompass.
Sodium starch octenylsuccinate 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 Sodium starch octenylsuccinate 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 Sodium starch octenylsuccinate GMP manufacturer or Sodium starch octenylsuccinate GMP API supplier for your needs.
A Sodium starch octenylsuccinate CoA (Certificate of Analysis) is a formal document that attests to Sodium starch octenylsuccinate's compliance with Sodium starch octenylsuccinate specifications and serves as a tool for batch-level quality control.
Sodium starch octenylsuccinate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium starch octenylsuccinate 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.
Sodium starch octenylsuccinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium starch octenylsuccinate EP), Sodium starch octenylsuccinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium starch octenylsuccinate USP).