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1. Schembl797992
2. Ndi5001
3. Ndi-5001
4. 1,1'-(1,12-dodecanediyl)bis[cyclopropanecarboxylic Acid]
5. Cyclopropanecarboxylic Acid, 1,1'-(1,12-dodecanediyl)bis-
6. 1-[12-(1 Carboxycyclopropyl)dodecyl]cyclopropane-1-carboxylic Acid
7. 1365571-66-9
| Molecular Weight | 338.5 g/mol |
|---|---|
| Molecular Formula | C20H34O4 |
| XLogP3 | 6 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 15 |
| Exact Mass | g/mol |
| Monoisotopic Mass | g/mol |
| Topological Polar Surface Area | 74.6 |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 381 |
| 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 |
Drugs in Development
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PharmaCompass offers a list of NDI-5001 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 NDI-5001 manufacturer or NDI-5001 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred NDI-5001 manufacturer or NDI-5001 supplier.
PharmaCompass also assists you with knowing the NDI-5001 API Price utilized in the formulation of products. NDI-5001 API Price is not always fixed or binding as the NDI-5001 Price is obtained through a variety of data sources. The NDI-5001 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NDI-5001 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NDI-5001, including repackagers and relabelers. The FDA regulates NDI-5001 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NDI-5001 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 NDI-5001 supplier is an individual or a company that provides NDI-5001 active pharmaceutical ingredient (API) or NDI-5001 finished formulations upon request. The NDI-5001 suppliers may include NDI-5001 API manufacturers, exporters, distributors and traders.
NDI-5001 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 NDI-5001 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 NDI-5001 GMP manufacturer or NDI-5001 GMP API supplier for your needs.
A NDI-5001 CoA (Certificate of Analysis) is a formal document that attests to NDI-5001's compliance with NDI-5001 specifications and serves as a tool for batch-level quality control.
NDI-5001 CoA mostly includes findings from lab analyses of a specific batch. For each NDI-5001 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.
NDI-5001 may be tested according to a variety of international standards, such as European Pharmacopoeia (NDI-5001 EP), NDI-5001 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NDI-5001 USP).
