Synopsis
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CEP/COS
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NDC API
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USP
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JP
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FDA Orange Book
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| Molecular Weight | 315.29 g/mol |
|---|---|
| Molecular Formula | C10H17N7O5 |
| XLogP3 | -4.3 |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 3 |
| Exact Mass | 315.12911667 g/mol |
| Monoisotopic Mass | 315.12911667 g/mol |
| Topological Polar Surface Area | 194 A^2 |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 566 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Neosaxitoxin 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 Neosaxitoxin manufacturer or Neosaxitoxin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Neosaxitoxin manufacturer or Neosaxitoxin supplier.
PharmaCompass also assists you with knowing the Neosaxitoxin API Price utilized in the formulation of products. Neosaxitoxin API Price is not always fixed or binding as the Neosaxitoxin Price is obtained through a variety of data sources. The Neosaxitoxin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neosaxitoxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neosaxitoxin, including repackagers and relabelers. The FDA regulates Neosaxitoxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neosaxitoxin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Neosaxitoxin supplier is an individual or a company that provides Neosaxitoxin active pharmaceutical ingredient (API) or Neosaxitoxin finished formulations upon request. The Neosaxitoxin suppliers may include Neosaxitoxin API manufacturers, exporters, distributors and traders.
click here to find a list of Neosaxitoxin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Neosaxitoxin DMF (Drug Master File) is a document detailing the whole manufacturing process of Neosaxitoxin active pharmaceutical ingredient (API) in detail. Different forms of Neosaxitoxin DMFs exist exist since differing nations have different regulations, such as Neosaxitoxin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Neosaxitoxin DMF submitted to regulatory agencies in the US is known as a USDMF. Neosaxitoxin USDMF includes data on Neosaxitoxin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Neosaxitoxin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Neosaxitoxin suppliers with USDMF on PharmaCompass.
Neosaxitoxin 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 Neosaxitoxin 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 Neosaxitoxin GMP manufacturer or Neosaxitoxin GMP API supplier for your needs.
A Neosaxitoxin CoA (Certificate of Analysis) is a formal document that attests to Neosaxitoxin's compliance with Neosaxitoxin specifications and serves as a tool for batch-level quality control.
Neosaxitoxin CoA mostly includes findings from lab analyses of a specific batch. For each Neosaxitoxin 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.
Neosaxitoxin may be tested according to a variety of international standards, such as European Pharmacopoeia (Neosaxitoxin EP), Neosaxitoxin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Neosaxitoxin USP).
