Synopsis
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1. Schembl3694818
| Molecular Weight | 526.6 g/mol |
|---|---|
| Molecular Formula | C24H34N2O9S |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 9 |
| Exact Mass | 526.19850184 g/mol |
| Monoisotopic Mass | 526.19850184 g/mol |
| Topological Polar Surface Area | 185 Ų |
| Heavy Atom Count | 36 |
| Formal Charge | 0 |
| Complexity | 641 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
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PharmaCompass offers a list of Bedoradrine 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 Bedoradrine manufacturer or Bedoradrine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bedoradrine manufacturer or Bedoradrine supplier.
PharmaCompass also assists you with knowing the Bedoradrine API Price utilized in the formulation of products. Bedoradrine API Price is not always fixed or binding as the Bedoradrine Price is obtained through a variety of data sources. The Bedoradrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bedoradrine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bedoradrine, including repackagers and relabelers. The FDA regulates Bedoradrine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bedoradrine 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 Bedoradrine supplier is an individual or a company that provides Bedoradrine active pharmaceutical ingredient (API) or Bedoradrine finished formulations upon request. The Bedoradrine suppliers may include Bedoradrine API manufacturers, exporters, distributors and traders.
click here to find a list of Bedoradrine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Bedoradrine DMF (Drug Master File) is a document detailing the whole manufacturing process of Bedoradrine active pharmaceutical ingredient (API) in detail. Different forms of Bedoradrine DMFs exist exist since differing nations have different regulations, such as Bedoradrine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Bedoradrine DMF submitted to regulatory agencies in the US is known as a USDMF. Bedoradrine USDMF includes data on Bedoradrine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Bedoradrine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Bedoradrine suppliers with USDMF on PharmaCompass.
Bedoradrine 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 Bedoradrine 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 Bedoradrine GMP manufacturer or Bedoradrine GMP API supplier for your needs.
A Bedoradrine CoA (Certificate of Analysis) is a formal document that attests to Bedoradrine's compliance with Bedoradrine specifications and serves as a tool for batch-level quality control.
Bedoradrine CoA mostly includes findings from lab analyses of a specific batch. For each Bedoradrine 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.
Bedoradrine may be tested according to a variety of international standards, such as European Pharmacopoeia (Bedoradrine EP), Bedoradrine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Bedoradrine USP).
