Synopsis
Synopsis
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CEP/COS
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JDMF
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NDC API
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VMF
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Listed Suppliers
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USP
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JP
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FDF Dossiers
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FDA Orange Book
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Europe
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| Molecular Weight | 702.0 g/mol |
|---|---|
| Molecular Formula | C39H67N5O6 |
| XLogP3 | 5.2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 20 |
| Exact Mass | 701.50913487 g/mol |
| Monoisotopic Mass | 701.50913487 g/mol |
| Topological Polar Surface Area | 121 A^2 |
| Heavy Atom Count | 50 |
| Formal Charge | 0 |
| Complexity | 1060 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 8 |
| 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 Soblidotin 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 Soblidotin manufacturer or Soblidotin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Soblidotin manufacturer or Soblidotin supplier.
PharmaCompass also assists you with knowing the Soblidotin API Price utilized in the formulation of products. Soblidotin API Price is not always fixed or binding as the Soblidotin Price is obtained through a variety of data sources. The Soblidotin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Soblidotin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Soblidotin, including repackagers and relabelers. The FDA regulates Soblidotin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Soblidotin 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 Soblidotin supplier is an individual or a company that provides Soblidotin active pharmaceutical ingredient (API) or Soblidotin finished formulations upon request. The Soblidotin suppliers may include Soblidotin API manufacturers, exporters, distributors and traders.
click here to find a list of Soblidotin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Soblidotin DMF (Drug Master File) is a document detailing the whole manufacturing process of Soblidotin active pharmaceutical ingredient (API) in detail. Different forms of Soblidotin DMFs exist exist since differing nations have different regulations, such as Soblidotin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Soblidotin DMF submitted to regulatory agencies in the US is known as a USDMF. Soblidotin USDMF includes data on Soblidotin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Soblidotin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Soblidotin suppliers with USDMF on PharmaCompass.
Soblidotin 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 Soblidotin 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 Soblidotin GMP manufacturer or Soblidotin GMP API supplier for your needs.
A Soblidotin CoA (Certificate of Analysis) is a formal document that attests to Soblidotin's compliance with Soblidotin specifications and serves as a tool for batch-level quality control.
Soblidotin CoA mostly includes findings from lab analyses of a specific batch. For each Soblidotin 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.
Soblidotin may be tested according to a variety of international standards, such as European Pharmacopoeia (Soblidotin EP), Soblidotin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Soblidotin USP).
