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1. Dfp-10917
1. Dfp-10917
2. Schembl20459902
3. Sb18699
| Molecular Weight | 252.23 g/mol |
|---|---|
| Molecular Formula | C10H12N4O4 |
| XLogP3 | -2.4 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 2 |
| Exact Mass | 252.08585488 g/mol |
| Monoisotopic Mass | 252.08585488 g/mol |
| Topological Polar Surface Area | 132 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 466 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 4 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A DFP-10917 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DFP-10917, including repackagers and relabelers. The FDA regulates DFP-10917 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DFP-10917 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 DFP-10917 supplier is an individual or a company that provides DFP-10917 active pharmaceutical ingredient (API) or DFP-10917 finished formulations upon request. The DFP-10917 suppliers may include DFP-10917 API manufacturers, exporters, distributors and traders.
DFP-10917 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 DFP-10917 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 DFP-10917 GMP manufacturer or DFP-10917 GMP API supplier for your needs.
A DFP-10917 CoA (Certificate of Analysis) is a formal document that attests to DFP-10917's compliance with DFP-10917 specifications and serves as a tool for batch-level quality control.
DFP-10917 CoA mostly includes findings from lab analyses of a specific batch. For each DFP-10917 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.
DFP-10917 may be tested according to a variety of international standards, such as European Pharmacopoeia (DFP-10917 EP), DFP-10917 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DFP-10917 USP).
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