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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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
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
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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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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FDF Dossiers
Regulatory Info :
Registration Country : India
Metamizole Magnesium; Pargeverine
Brand Name :
Dosage Form : Oral Drops
Dosage Strength : 300MG/ML; 6MG/ML
Packaging : 15 ml PET Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Solution for Oral Drops
Dosage Strength : 5MG/ML
Packaging : 200 ml amber Bottle pack
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Dossiers
Regulatory Info :
Registration Country : India
Metamizole Magnesium; Pargeverine
Brand Name :
Dosage Form : Oral Drops
Dosage Strength : 300MG/ML; 6MG/ML
Packaging : 15 ml PET Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Packaging : 15 ml PET Bottle
Regulatory Info :
Metamizole Magnesium; Pargeverine
Dosage : Oral Drops
Dosage Strength : 300MG/ML; 6MG/ML
Brand Name :
Approval Date :
Application Number :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Solution for Oral Drop...
Dosage Strength : 5MG/ML
Packaging : 200 ml amber Bottle pack
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Packaging : 200 ml amber Bottle pack
Regulatory Info :
Dosage : Solution for Oral Drop...
Dosage Strength : 5MG/ML
Brand Name :
Approval Date :
Application Number :
Registration Country : India
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
ABOUT THIS PAGE
90
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 Pargeverina [INN-Spanish] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pargeverina [INN-Spanish], including repackagers and relabelers. The FDA regulates Pargeverina [INN-Spanish] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pargeverina [INN-Spanish] 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 Pargeverina [INN-Spanish] manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pargeverina [INN-Spanish] supplier is an individual or a company that provides Pargeverina [INN-Spanish] active pharmaceutical ingredient (API) or Pargeverina [INN-Spanish] finished formulations upon request. The Pargeverina [INN-Spanish] suppliers may include Pargeverina [INN-Spanish] API manufacturers, exporters, distributors and traders.
click here to find a list of Pargeverina [INN-Spanish] suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Pargeverina [INN-Spanish] 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 Pargeverina [INN-Spanish] 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 Pargeverina [INN-Spanish] GMP manufacturer or Pargeverina [INN-Spanish] GMP API supplier for your needs.
A Pargeverina [INN-Spanish] CoA (Certificate of Analysis) is a formal document that attests to Pargeverina [INN-Spanish]'s compliance with Pargeverina [INN-Spanish] specifications and serves as a tool for batch-level quality control.
Pargeverina [INN-Spanish] CoA mostly includes findings from lab analyses of a specific batch. For each Pargeverina [INN-Spanish] 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.
Pargeverina [INN-Spanish] may be tested according to a variety of international standards, such as European Pharmacopoeia (Pargeverina [INN-Spanish] EP), Pargeverina [INN-Spanish] JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Pargeverina [INN-Spanish] USP).
