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
1. 19094-56-5
2. Benzoic Acid, 2-chloro-5-iodo-
3. 2-chloro-5-iodo-benzoic Acid
4. Mfcd00079731
5. 2-chloro-5-iodobenzoicacid
6. Ec 606-224-0
7. 5-iodo-2-chlorobenzoic Acid
8. Schembl305505
9. Dtxsid00334099
10. Act07777
11. Cs-d1207
12. Str08177
13. Zinc2149847
14. 2-chloro-5-iodobenzoic Acid, 97%
15. Lt0050
16. Stl377354
17. Akos002341055
18. Ac-3935
19. Ps-7223
20. Sy006737
21. Db-014080
22. Am20030244
23. Ft-0611823
24. A19981
25. J-508849
26. Z1416282584
| Molecular Weight | 282.46 g/mol |
|---|---|
| Molecular Formula | C7H4ClIO2 |
| XLogP3 | 2.8 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 281.89445 g/mol |
| Monoisotopic Mass | 281.89445 g/mol |
| Topological Polar Surface Area | 37.3 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 163 |
| 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 |
ABOUT THIS PAGE
18
PharmaCompass offers a list of LT0050 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 LT0050 manufacturer or LT0050 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred LT0050 manufacturer or LT0050 supplier.
PharmaCompass also assists you with knowing the LT0050 API Price utilized in the formulation of products. LT0050 API Price is not always fixed or binding as the LT0050 Price is obtained through a variety of data sources. The LT0050 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LT0050 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LT0050, including repackagers and relabelers. The FDA regulates LT0050 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LT0050 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 LT0050 supplier is an individual or a company that provides LT0050 active pharmaceutical ingredient (API) or LT0050 finished formulations upon request. The LT0050 suppliers may include LT0050 API manufacturers, exporters, distributors and traders.
LT0050 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 LT0050 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 LT0050 GMP manufacturer or LT0050 GMP API supplier for your needs.
A LT0050 CoA (Certificate of Analysis) is a formal document that attests to LT0050's compliance with LT0050 specifications and serves as a tool for batch-level quality control.
LT0050 CoA mostly includes findings from lab analyses of a specific batch. For each LT0050 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.
LT0050 may be tested according to a variety of international standards, such as European Pharmacopoeia (LT0050 EP), LT0050 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (LT0050 USP).
