Synopsis
Synopsis
0
API Suppliers
0
USDMF
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
| Molecular Weight | 560.0 g/mol |
|---|---|
| Molecular Formula | C19H18ClN5O7S3 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 9 |
| Exact Mass | 559.0056891 g/mol |
| Monoisotopic Mass | 559.0056891 g/mol |
| Topological Polar Surface Area | 256 Ų |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 945 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 3 |
ABOUT THIS PAGE
81
PharmaCompass offers a list of I06-1292 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 I06-1292 manufacturer or I06-1292 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred I06-1292 manufacturer or I06-1292 supplier.
PharmaCompass also assists you with knowing the I06-1292 API Price utilized in the formulation of products. I06-1292 API Price is not always fixed or binding as the I06-1292 Price is obtained through a variety of data sources. The I06-1292 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A I06-1292 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of I06-1292, including repackagers and relabelers. The FDA regulates I06-1292 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. I06-1292 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 I06-1292 supplier is an individual or a company that provides I06-1292 active pharmaceutical ingredient (API) or I06-1292 finished formulations upon request. The I06-1292 suppliers may include I06-1292 API manufacturers, exporters, distributors and traders.
I06-1292 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 I06-1292 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 I06-1292 GMP manufacturer or I06-1292 GMP API supplier for your needs.
A I06-1292 CoA (Certificate of Analysis) is a formal document that attests to I06-1292's compliance with I06-1292 specifications and serves as a tool for batch-level quality control.
I06-1292 CoA mostly includes findings from lab analyses of a specific batch. For each I06-1292 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.
I06-1292 may be tested according to a variety of international standards, such as European Pharmacopoeia (I06-1292 EP), I06-1292 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (I06-1292 USP).
