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
API
0
FDF
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
1. Vmm
2. Gtpl11753
3. Etx-0462
4. (4r,7s)-7-(n'-hydroxy-n-methylcarbamimidoyl)-1-methyl-4-[(sulfooxy)amino]-1,4,5,7-tetrahydro-6h-pyrazolo[3,4-c]pyridine-6-carboxylic Acid
| Molecular Weight | 364.34 g/mol |
|---|---|
| Molecular Formula | C10H16N6O7S |
| XLogP3 | -5.1 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 5 |
| Exact Mass | 364.08011804 g/mol |
| Monoisotopic Mass | 364.08011804 g/mol |
| Topological Polar Surface Area | 187 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 607 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
A ETX0462 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ETX0462, including repackagers and relabelers. The FDA regulates ETX0462 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ETX0462 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 ETX0462 supplier is an individual or a company that provides ETX0462 active pharmaceutical ingredient (API) or ETX0462 finished formulations upon request. The ETX0462 suppliers may include ETX0462 API manufacturers, exporters, distributors and traders.
ETX0462 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 ETX0462 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 ETX0462 GMP manufacturer or ETX0462 GMP API supplier for your needs.
A ETX0462 CoA (Certificate of Analysis) is a formal document that attests to ETX0462's compliance with ETX0462 specifications and serves as a tool for batch-level quality control.
ETX0462 CoA mostly includes findings from lab analyses of a specific batch. For each ETX0462 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.
ETX0462 may be tested according to a variety of international standards, such as European Pharmacopoeia (ETX0462 EP), ETX0462 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (ETX0462 USP).
LOOKING FOR A SUPPLIER?
