Synopsis
Synopsis
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USDMF
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CEP/COS
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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Others
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
US Medicaid
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Annual Reports
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Regulatory FDF Prices
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FDF
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Data Compilation #PharmaFlow
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1. Propinox
2. Propinoxate
1. Propinox
2. 13479-13-5
3. Pargeverine [inn]
4. Pargeverine Hcl
5. Pargeverin
6. Viadil
7. 2-(dimethylamino)ethyl 2,2-diphenyl-2-prop-2-ynoxyacetate
8. Uc61hm8fx0
9. Diphenyl(2-propynyloxy)acetic Acid 2-(dimethylamino)ethyl Ester
10. Pargeverine (inn)
11. 2-(dimethylamino)ethyl Diphenyl(2-propynyloxy)acetate
12. Terisal
13. Acetic Acid, Diphenyl(2-propynyloxy)-, 2-(dimethylamino)ethyl Ester
14. Pargeverina
15. Pargeverinum
16. Pargeverinum [inn-latin]
17. Pargeverina [inn-spanish]
18. Be 50
19. Ncgc00164558-01
20. Unii-uc61hm8fx0
21. Brn 2226014
22. Viadil (tn)
23. Pargevarine Hcl
24. Benzeneacetic Acid, Alpha-phenyl-alpha-(2-propynyloxy)-, 2-(dimethylamino)ethyl Ester
25. Pargeverine [who-dd]
26. Schembl2111437
27. Chembl1872101
28. Dtxsid1048386
29. Chebi:135433
30. Zinc2019610
31. D07466
32. Q27291011
33. Benzeneacetic Acid, .alpha.-phenyl-.alpha.-(2-propynyloxy)-, 2-(dimethylamino)ethyl Ester
| Molecular Weight | 337.4 g/mol |
|---|---|
| Molecular Formula | C21H23NO3 |
| XLogP3 | 3.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 9 |
| Exact Mass | 337.16779360 g/mol |
| Monoisotopic Mass | 337.16779360 g/mol |
| Topological Polar Surface Area | 38.8 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 435 |
| 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 |
API SUPPLIERS
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Listed Suppliers
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
About the Company : MINAKEM is a cGMP custom manufacturer of small molecule API, HPAPI and steroids. All development and manufacturing activities are supported by highly skilled R&D teams, supported b...
Minakem is manufacturing small molecules APIs including corticosteroids
About the Company : Minakem Montreal is developing and manufacturing small molecules APIs and advanced intermediates, including corticosteroids. Following efficient processes and methodologies, our em...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
About the Company : Established in 1984, R L Fine Chem Pvt. Ltd. is one of the fastest growing API companies, with a leadership position in several APIs such as antihistamines, antidepressants and mus...
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ABOUT THIS PAGE
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PharmaCompass offers a list of Pargeverine 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 Pargeverine manufacturer or Pargeverine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pargeverine manufacturer or Pargeverine supplier.
PharmaCompass also assists you with knowing the Pargeverine API Price utilized in the formulation of products. Pargeverine API Price is not always fixed or binding as the Pargeverine Price is obtained through a variety of data sources. The Pargeverine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PARGEVERINE HCL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PARGEVERINE HCL, including repackagers and relabelers. The FDA regulates PARGEVERINE HCL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PARGEVERINE HCL 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 PARGEVERINE HCL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PARGEVERINE HCL supplier is an individual or a company that provides PARGEVERINE HCL active pharmaceutical ingredient (API) or PARGEVERINE HCL finished formulations upon request. The PARGEVERINE HCL suppliers may include PARGEVERINE HCL API manufacturers, exporters, distributors and traders.
click here to find a list of PARGEVERINE HCL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
PARGEVERINE HCL 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 PARGEVERINE HCL 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 PARGEVERINE HCL GMP manufacturer or PARGEVERINE HCL GMP API supplier for your needs.
A PARGEVERINE HCL CoA (Certificate of Analysis) is a formal document that attests to PARGEVERINE HCL's compliance with PARGEVERINE HCL specifications and serves as a tool for batch-level quality control.
PARGEVERINE HCL CoA mostly includes findings from lab analyses of a specific batch. For each PARGEVERINE HCL 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.
PARGEVERINE HCL may be tested according to a variety of international standards, such as European Pharmacopoeia (PARGEVERINE HCL EP), PARGEVERINE HCL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (PARGEVERINE HCL USP).
