Synopsis
Synopsis
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CEP/COS
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1. Vasoklin
2. Opilon
3. M-101
4. Moxisylyte Hcl
5. Wv 365
6. Wk2kzm9v6x
7. Enfrental
8. Limatene
9. 2-(4-acetyloxy-5-methyl-2-propan-2-ylphenoxy)ethyl-dimethylazanium;chloride
10. [4-[2-(dimethylamino)ethoxy]-2-methyl-5-propan-2-ylphenyl] Acetate;hydron;chloride
11. 5-(2-(n,n-dimethylamino)ethoxy)carvacrol Acetate Hydrochloride
12. Einecs 213-519-4
13. Nsc 170448
14. Unii-wk2kzm9v6x
15. Dtxsid9046946
16. Chlorhydrate De Acetoxy-thymoxy-ethyl-dimethylamine [french]
17. (2-(4-acetoxy-2-isopropyl-5-methylphenoxy)ethyl)dimethylamine Hydrochloride
18. Carvacrol, 5-(2-(dimethylamino)ethoxy)-, Acetate (ester), Hydrochloride
19. Carvacrol, 5-(2-(n,n-dimethylamino)ethoxy)-, Acetate, Hydrochloride
20. Phenol, 4-(2-(dimethylamino)ethoxy)-2-methyl-5-(1-methylethyl)-, Acetate (ester), Hydrochloride
21. Chlorhydrate De Acetoxy-thymoxy-ethyl-dimethylamine
| Molecular Weight | 315.83 g/mol |
|---|---|
| Molecular Formula | C16H26ClNO3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 7 |
| Exact Mass | 315.1601214 g/mol |
| Monoisotopic Mass | 315.1601214 g/mol |
| Topological Polar Surface Area | 40 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 304 |
| 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
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PharmaCompass offers a list of Arlitene 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 Arlitene manufacturer or Arlitene supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Arlitene manufacturer or Arlitene supplier.
PharmaCompass also assists you with knowing the Arlitene API Price utilized in the formulation of products. Arlitene API Price is not always fixed or binding as the Arlitene Price is obtained through a variety of data sources. The Arlitene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Carlytene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carlytene, including repackagers and relabelers. The FDA regulates Carlytene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carlytene 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 Carlytene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Carlytene supplier is an individual or a company that provides Carlytene active pharmaceutical ingredient (API) or Carlytene finished formulations upon request. The Carlytene suppliers may include Carlytene API manufacturers, exporters, distributors and traders.
click here to find a list of Carlytene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Carlytene DMF (Drug Master File) is a document detailing the whole manufacturing process of Carlytene active pharmaceutical ingredient (API) in detail. Different forms of Carlytene DMFs exist exist since differing nations have different regulations, such as Carlytene USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Carlytene DMF submitted to regulatory agencies in the US is known as a USDMF. Carlytene USDMF includes data on Carlytene's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Carlytene USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Carlytene suppliers with USDMF on PharmaCompass.
Carlytene 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 Carlytene 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 Carlytene GMP manufacturer or Carlytene GMP API supplier for your needs.
A Carlytene CoA (Certificate of Analysis) is a formal document that attests to Carlytene's compliance with Carlytene specifications and serves as a tool for batch-level quality control.
Carlytene CoA mostly includes findings from lab analyses of a specific batch. For each Carlytene 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.
Carlytene may be tested according to a variety of international standards, such as European Pharmacopoeia (Carlytene EP), Carlytene JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Carlytene USP).
