Synopsis
Synopsis
0
USDMF
0
CEP/COS
0
JDMF
0
KDMF
0
NDC API
0
VMF
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. 14777-25-4
2. 10-[3-(4-methylpiperazin-1-yl)propyl]-10h-phenothiazine Dimalonate
3. 94ll6t81ri
4. 10-[3-(4-methylpiperazin-1-yl)propyl]phenothiazine;propanedioic Acid
5. Perazine Dimalonate (jan)
6. Perazine Dimalonate [jan]
7. 10-(3-(4-methylpiperazin-1-yl)propyl)-10h-phenothiazine Dimalonate
8. Unii-94ll6t81ri
9. Einecs 238-842-8
10. Chebi:31978
11. Dtxsid70163797
12. Perazine Dimalonate [mart.]
13. Perazine Dimalonate [who-dd]
14. D01860
15. Q27271688
| Molecular Weight | 547.6 g/mol |
|---|---|
| Molecular Formula | C26H33N3O8S |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 8 |
| Exact Mass | 547.19883619 g/mol |
| Monoisotopic Mass | 547.19883619 g/mol |
| Topological Polar Surface Area | 184 Ų |
| Heavy Atom Count | 38 |
| Formal Charge | 0 |
| Complexity | 458 |
| 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 | 3 |
ABOUT THIS PAGE
A Perazine Dimalonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Perazine Dimalonate, including repackagers and relabelers. The FDA regulates Perazine Dimalonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Perazine Dimalonate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Perazine Dimalonate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Perazine Dimalonate supplier is an individual or a company that provides Perazine Dimalonate active pharmaceutical ingredient (API) or Perazine Dimalonate finished formulations upon request. The Perazine Dimalonate suppliers may include Perazine Dimalonate API manufacturers, exporters, distributors and traders.
click here to find a list of Perazine Dimalonate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Perazine Dimalonate written confirmation (Perazine Dimalonate WC) is an official document issued by a regulatory agency to a Perazine Dimalonate manufacturer, verifying that the manufacturing facility of a Perazine Dimalonate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Perazine Dimalonate APIs or Perazine Dimalonate finished pharmaceutical products to another nation, regulatory agencies frequently require a Perazine Dimalonate WC (written confirmation) as part of the regulatory process.
click here to find a list of Perazine Dimalonate suppliers with Written Confirmation (WC) on PharmaCompass.
Perazine Dimalonate 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 Perazine Dimalonate 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 Perazine Dimalonate GMP manufacturer or Perazine Dimalonate GMP API supplier for your needs.
A Perazine Dimalonate CoA (Certificate of Analysis) is a formal document that attests to Perazine Dimalonate's compliance with Perazine Dimalonate specifications and serves as a tool for batch-level quality control.
Perazine Dimalonate CoA mostly includes findings from lab analyses of a specific batch. For each Perazine Dimalonate 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.
Perazine Dimalonate may be tested according to a variety of international standards, such as European Pharmacopoeia (Perazine Dimalonate EP), Perazine Dimalonate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Perazine Dimalonate USP).
LOOKING FOR A SUPPLIER?
