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1. 98243-58-4
2. Verticillatine (rauwolfia)
3. Dtxsid70913355
4. 18-norsarpaganium, 17,19-epoxy-19,20-dihydro-10,17-dihydroxy-4,21-dimethyl-, (20beta)-
Molecular Weight | 341.4 g/mol |
---|---|
Molecular Formula | C20H25N2O3+ |
XLogP3 | 1.9 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 0 |
Exact Mass | 341.18651766 g/mol |
Monoisotopic Mass | 341.18651766 g/mol |
Topological Polar Surface Area | 65.5 Ų |
Heavy Atom Count | 25 |
Formal Charge | 1 |
Complexity | 587 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 8 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
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PharmaCompass offers a list of Verticillatine 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 Verticillatine manufacturer or Verticillatine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Verticillatine manufacturer or Verticillatine supplier.
PharmaCompass also assists you with knowing the Verticillatine API Price utilized in the formulation of products. Verticillatine API Price is not always fixed or binding as the Verticillatine Price is obtained through a variety of data sources. The Verticillatine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rauwolfia Serpentina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rauwolfia Serpentina, including repackagers and relabelers. The FDA regulates Rauwolfia Serpentina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rauwolfia Serpentina 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 Rauwolfia Serpentina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rauwolfia Serpentina supplier is an individual or a company that provides Rauwolfia Serpentina active pharmaceutical ingredient (API) or Rauwolfia Serpentina finished formulations upon request. The Rauwolfia Serpentina suppliers may include Rauwolfia Serpentina API manufacturers, exporters, distributors and traders.
click here to find a list of Rauwolfia Serpentina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rauwolfia Serpentina DMF (Drug Master File) is a document detailing the whole manufacturing process of Rauwolfia Serpentina active pharmaceutical ingredient (API) in detail. Different forms of Rauwolfia Serpentina DMFs exist exist since differing nations have different regulations, such as Rauwolfia Serpentina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rauwolfia Serpentina DMF submitted to regulatory agencies in the US is known as a USDMF. Rauwolfia Serpentina USDMF includes data on Rauwolfia Serpentina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rauwolfia Serpentina USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Rauwolfia Serpentina suppliers with USDMF on PharmaCompass.
Rauwolfia Serpentina 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 Rauwolfia Serpentina 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 Rauwolfia Serpentina GMP manufacturer or Rauwolfia Serpentina GMP API supplier for your needs.
A Rauwolfia Serpentina CoA (Certificate of Analysis) is a formal document that attests to Rauwolfia Serpentina's compliance with Rauwolfia Serpentina specifications and serves as a tool for batch-level quality control.
Rauwolfia Serpentina CoA mostly includes findings from lab analyses of a specific batch. For each Rauwolfia Serpentina 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.
Rauwolfia Serpentina may be tested according to a variety of international standards, such as European Pharmacopoeia (Rauwolfia Serpentina EP), Rauwolfia Serpentina JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rauwolfia Serpentina USP).