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1. Retandrol
2. Testosterone 17-phenylpropionate
1. 1255-49-8
2. Retandrol
3. Testosterone 17-phenylpropionate
4. Testosterone Hydrocinnamate
5. Testosterone Phenpropionate
6. Testosterone, Hydrocinnamate
7. Testolent
8. [(8r,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] 3-phenylpropanoate
9. Androst-4-en-3-one, 17-(1-oxo-3-phenylpropoxy)-, (17beta)-
10. 17beta-hydroxyandrost-4-en-3-one 3-phenylpropionate
11. 8gn84gwx51
12. Chebi:35002
13. Nsc-26643
14. (8r,9s,10r,13s,14s,17s)-10,13-dimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl 3-phenylpropanoate
15. Einecs 215-014-4
16. Nsc 26643
17. Unii-8gn84gwx51
18. Ncgc00160504-01
19. Testanon 50 (tn)
20. Testosteron Phenylpropionate
21. Dsstox_cid_28638
22. Dsstox_rid_82908
23. Dsstox_gsid_48712
24. Schembl940358
25. Gtpl7628
26. Chembl2356993
27. Dtxsid5048712
28. Testosterone 17beta-phenpropionate
29. Androst-4-en-3-one, 17-(1-oxo-3-phenylpropoxy)-, (17-beta)-
30. Nsc26643
31. Zinc3881605
32. Tox21_113116
33. Androst-4-en-3-one, 17-(1-oxo-3-phenylpropoxy)-, (17.beta.)-
34. Mfcd00056484
35. Testosterone Phenyl Propionate
36. Akos015895428
37. Am84364
38. Ds-5641
39. Fd12013
40. Ac-28714
41. Cas-1255-49-8
42. Testosterone Phenylpropionate [mart.]
43. Testosterone Phenylpropionate [who-dd]
44. 3-oxoandrost-4-en-17-yl 3-phenylpropanoate #
45. D08574
46. 255t498
47. 4-androsten-17beta-ol-3-one 17-phenylpropionate
48. A805391
49. W-108401
50. Q27088964
51. Testosterone 17-phenylpropionate, Analytical Standard
52. 3-oxoandrost-4-en-17.beta.-yl 3-phenylpropionate
53. 17.beta.-hydroxyandrost-4-en-3-one 3-phenylpropionate
54. Androst-4-en-3-one, 17-(1-oxo-3-phenylpropoxy)-, (17?)-
Molecular Weight | 420.6 g/mol |
---|---|
Molecular Formula | C28H36O3 |
XLogP3 | 5.8 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 5 |
Exact Mass | 420.26644501 g/mol |
Monoisotopic Mass | 420.26644501 g/mol |
Topological Polar Surface Area | 43.4 Ų |
Heavy Atom Count | 31 |
Formal Charge | 0 |
Complexity | 747 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 6 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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ABOUT THIS PAGE
A Testosterone Phenylpropionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Testosterone Phenylpropionate, including repackagers and relabelers. The FDA regulates Testosterone Phenylpropionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Testosterone Phenylpropionate 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 Testosterone Phenylpropionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Testosterone Phenylpropionate supplier is an individual or a company that provides Testosterone Phenylpropionate active pharmaceutical ingredient (API) or Testosterone Phenylpropionate finished formulations upon request. The Testosterone Phenylpropionate suppliers may include Testosterone Phenylpropionate API manufacturers, exporters, distributors and traders.
click here to find a list of Testosterone Phenylpropionate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Testosterone Phenylpropionate written confirmation (Testosterone Phenylpropionate WC) is an official document issued by a regulatory agency to a Testosterone Phenylpropionate manufacturer, verifying that the manufacturing facility of a Testosterone Phenylpropionate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Testosterone Phenylpropionate APIs or Testosterone Phenylpropionate finished pharmaceutical products to another nation, regulatory agencies frequently require a Testosterone Phenylpropionate WC (written confirmation) as part of the regulatory process.
click here to find a list of Testosterone Phenylpropionate suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Testosterone Phenylpropionate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Testosterone Phenylpropionate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Testosterone Phenylpropionate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Testosterone Phenylpropionate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Testosterone Phenylpropionate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Testosterone Phenylpropionate suppliers with NDC on PharmaCompass.
Testosterone Phenylpropionate 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 Testosterone Phenylpropionate 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 Testosterone Phenylpropionate GMP manufacturer or Testosterone Phenylpropionate GMP API supplier for your needs.
A Testosterone Phenylpropionate CoA (Certificate of Analysis) is a formal document that attests to Testosterone Phenylpropionate's compliance with Testosterone Phenylpropionate specifications and serves as a tool for batch-level quality control.
Testosterone Phenylpropionate CoA mostly includes findings from lab analyses of a specific batch. For each Testosterone Phenylpropionate 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.
Testosterone Phenylpropionate may be tested according to a variety of international standards, such as European Pharmacopoeia (Testosterone Phenylpropionate EP), Testosterone Phenylpropionate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Testosterone Phenylpropionate USP).
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