Synopsis
Synopsis
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NDC API
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FDA Orange Book
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US Medicaid
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| Molecular Weight | 309.8 g/mol |
|---|---|
| Molecular Formula | C14H12ClNO3S |
| XLogP3 | 3.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 309.0226421 g/mol |
| Monoisotopic Mass | 309.0226421 g/mol |
| Topological Polar Surface Area | 97.6 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 371 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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 AC1OUEB9 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 AC1OUEB9 manufacturer or AC1OUEB9 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred AC1OUEB9 manufacturer or AC1OUEB9 supplier.
PharmaCompass also assists you with knowing the AC1OUEB9 API Price utilized in the formulation of products. AC1OUEB9 API Price is not always fixed or binding as the AC1OUEB9 Price is obtained through a variety of data sources. The AC1OUEB9 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AC1OUEB9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AC1OUEB9, including repackagers and relabelers. The FDA regulates AC1OUEB9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AC1OUEB9 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 AC1OUEB9 supplier is an individual or a company that provides AC1OUEB9 active pharmaceutical ingredient (API) or AC1OUEB9 finished formulations upon request. The AC1OUEB9 suppliers may include AC1OUEB9 API manufacturers, exporters, distributors and traders.
AC1OUEB9 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 AC1OUEB9 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 AC1OUEB9 GMP manufacturer or AC1OUEB9 GMP API supplier for your needs.
A AC1OUEB9 CoA (Certificate of Analysis) is a formal document that attests to AC1OUEB9's compliance with AC1OUEB9 specifications and serves as a tool for batch-level quality control.
AC1OUEB9 CoA mostly includes findings from lab analyses of a specific batch. For each AC1OUEB9 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.
AC1OUEB9 may be tested according to a variety of international standards, such as European Pharmacopoeia (AC1OUEB9 EP), AC1OUEB9 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AC1OUEB9 USP).
