Synopsis
Synopsis
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API Suppliers
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USDMF
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CEP/COS
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NDC API
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FDF
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FDF Dossiers
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FDA Orange Book
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Europe
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US Medicaid
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Molecular Weight | 379.4 g/mol |
---|---|
Molecular Formula | C20H29NO6-2 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 7 |
Rotatable Bond Count | 5 |
Exact Mass | 379.19948764 g/mol |
Monoisotopic Mass | 379.19948764 g/mol |
Topological Polar Surface Area | 124 Ų |
Heavy Atom Count | 27 |
Formal Charge | -2 |
Complexity | 348 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
ABOUT THIS PAGE
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PharmaCompass offers a list of O-Desmethyl-Venlafaxine Succinate 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 O-Desmethyl-Venlafaxine Succinate manufacturer or O-Desmethyl-Venlafaxine Succinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred O-Desmethyl-Venlafaxine Succinate manufacturer or O-Desmethyl-Venlafaxine Succinate supplier.
PharmaCompass also assists you with knowing the O-Desmethyl-Venlafaxine Succinate API Price utilized in the formulation of products. O-Desmethyl-Venlafaxine Succinate API Price is not always fixed or binding as the O-Desmethyl-Venlafaxine Succinate Price is obtained through a variety of data sources. The O-Desmethyl-Venlafaxine Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A O-Desmethyl-Venlafaxine Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of O-Desmethyl-Venlafaxine Succinate, including repackagers and relabelers. The FDA regulates O-Desmethyl-Venlafaxine Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. O-Desmethyl-Venlafaxine Succinate 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 O-Desmethyl-Venlafaxine Succinate supplier is an individual or a company that provides O-Desmethyl-Venlafaxine Succinate active pharmaceutical ingredient (API) or O-Desmethyl-Venlafaxine Succinate finished formulations upon request. The O-Desmethyl-Venlafaxine Succinate suppliers may include O-Desmethyl-Venlafaxine Succinate API manufacturers, exporters, distributors and traders.
O-Desmethyl-Venlafaxine Succinate 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 O-Desmethyl-Venlafaxine Succinate 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 O-Desmethyl-Venlafaxine Succinate GMP manufacturer or O-Desmethyl-Venlafaxine Succinate GMP API supplier for your needs.
A O-Desmethyl-Venlafaxine Succinate CoA (Certificate of Analysis) is a formal document that attests to O-Desmethyl-Venlafaxine Succinate's compliance with O-Desmethyl-Venlafaxine Succinate specifications and serves as a tool for batch-level quality control.
O-Desmethyl-Venlafaxine Succinate CoA mostly includes findings from lab analyses of a specific batch. For each O-Desmethyl-Venlafaxine Succinate 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.
O-Desmethyl-Venlafaxine Succinate may be tested according to a variety of international standards, such as European Pharmacopoeia (O-Desmethyl-Venlafaxine Succinate EP), O-Desmethyl-Venlafaxine Succinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (O-Desmethyl-Venlafaxine Succinate USP).