Synopsis
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| Molecular Weight | 288.30 g/mol |
|---|---|
| Molecular Formula | C14H16N4O3+2 |
| XLogP3 | 0.8 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 6 |
| Exact Mass | 288.12224039 g/mol |
| Monoisotopic Mass | 288.12224039 g/mol |
| Topological Polar Surface Area | 77.8 A^2 |
| Heavy Atom Count | 21 |
| Formal Charge | 2 |
| Complexity | 491 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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 Obidoxime 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 Obidoxime manufacturer or Obidoxime supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Obidoxime manufacturer or Obidoxime supplier.
PharmaCompass also assists you with knowing the Obidoxime API Price utilized in the formulation of products. Obidoxime API Price is not always fixed or binding as the Obidoxime Price is obtained through a variety of data sources. The Obidoxime Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Obidoxime manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Obidoxime, including repackagers and relabelers. The FDA regulates Obidoxime manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Obidoxime 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 Obidoxime supplier is an individual or a company that provides Obidoxime active pharmaceutical ingredient (API) or Obidoxime finished formulations upon request. The Obidoxime suppliers may include Obidoxime API manufacturers, exporters, distributors and traders.
Obidoxime 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 Obidoxime 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 Obidoxime GMP manufacturer or Obidoxime GMP API supplier for your needs.
A Obidoxime CoA (Certificate of Analysis) is a formal document that attests to Obidoxime's compliance with Obidoxime specifications and serves as a tool for batch-level quality control.
Obidoxime CoA mostly includes findings from lab analyses of a specific batch. For each Obidoxime 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.
Obidoxime may be tested according to a variety of international standards, such as European Pharmacopoeia (Obidoxime EP), Obidoxime JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Obidoxime USP).
