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. Luostyl
2. Difemerine Hcl
3. 70280-88-5
4. 00jm91q28f
5. 2-(dimethylamino)-1,1-dimethylethyl Diphenylglycolate Hydrochloride
6. [2-(dimethylamino)-2-methylpropyl] 2-hydroxy-2,2-diphenylacetate;hydrochloride
7. Difemerin Hydrochlorid
8. Unii-00jm91q28f
9. Dtxsid90220513
10. Einecs 274-526-6
11. Difemerine Hydrochloride [mi]
12. Up 0357
13. Difemerine Hydrochloride [mart.]
14. Difemerine Hydrochloride [who-dd]
15. Q27231355
16. 2-(dimethylamino)-1,1-dimethylethyl Benzilate, Hydrochloride
17. .alpha.-hydroxy-.alpha.-phenylbenzeneacetic Acid 2-(dimethylamino)-2-methylpropyl Ester, Hydrochloride
| Molecular Weight | 363.9 g/mol |
|---|---|
| Molecular Formula | C20H26ClNO3 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 7 |
| Exact Mass | 363.1601214 g/mol |
| Monoisotopic Mass | 363.1601214 g/mol |
| Topological Polar Surface Area | 49.8 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 389 |
| 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 | 2 |
ABOUT THIS PAGE
84
PharmaCompass offers a list of Difemerine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Difemerine Hydrochloride manufacturer or Difemerine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Difemerine Hydrochloride manufacturer or Difemerine Hydrochloride supplier.
A Luostyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Luostyl, including repackagers and relabelers. The FDA regulates Luostyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Luostyl 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 Luostyl supplier is an individual or a company that provides Luostyl active pharmaceutical ingredient (API) or Luostyl finished formulations upon request. The Luostyl suppliers may include Luostyl API manufacturers, exporters, distributors and traders.
Luostyl 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 Luostyl GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Luostyl GMP manufacturer or Luostyl GMP API supplier for your needs.
A Luostyl CoA (Certificate of Analysis) is a formal document that attests to Luostyl's compliance with Luostyl specifications and serves as a tool for batch-level quality control.
Luostyl CoA mostly includes findings from lab analyses of a specific batch. For each Luostyl 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.
Luostyl may be tested according to a variety of international standards, such as European Pharmacopoeia (Luostyl EP), Luostyl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Luostyl USP).
