Synopsis
Synopsis
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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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API
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FDF
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FDA Orange Book
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Europe
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Australia
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South Africa
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Patents
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US Exclusivities
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Health Canada Patents
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Data Compilation #PharmaFlow
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
US Medicaid
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Annual Reports
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Finished Drug Prices
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1. 17 Beta-acetoxyestra-4,9,11-trien-3-one
2. Acetate, Trenbolone
3. Acetate, Trienbolone
4. Progro T S
5. Progro T-s
6. Progro Ts
7. Trenbolone
8. Trenbolone Acetate, (17beta)-isomer
9. Trienbolone
10. Trienbolone Acetate
1. 10161-34-9
2. Finaplix
3. Trenbolone 17-acetate
4. Trenbolone (acetate)
5. Ru-1697
6. [(8s,13s,14s,17s)-13-methyl-3-oxo-2,6,7,8,14,15,16,17-octahydro-1h-cyclopenta[a]phenanthren-17-yl] Acetate
7. Trenbolone Acetate Ciii
8. Rud5y4sv0s
9. 17-beta-(acetyloxy)estra-4,9,11-trien-3-one
10. Trienbolone Acetate
11. Estra-4,9,11-trien-3-one, 17-(acetyloxy)-, (17b)-
12. Ncgc00167439-01
13. Component T-s
14. Finaplix H
15. Component T-h
16. Trenbolone Acetate [usan]
17. Einecs 233-432-5
18. Unii-rud5y4sv0s
19. Ru 1697
20. Brn 2012395
21. Estra-4,9,11-trien-3-one, 17-(acetyloxy)-, (17.beta.)-
22. 3-oxo-17beta-acetoxyestra-4,9,11-triene
23. Trenbolone Acetate [usan:usp]
24. Trenbolone-acetate
25. Finaplix (tn)
26. 17-beta-acetoxy-delta-4,9,11-estratrien-3-one
27. 17-beta-hydroxyestra-4,9,11-trien-3-one Acetate
28. 17beta-hydroxyestra-4,9,11-trien-3-one, Acetate
29. 17beta-hydroxyestra-4,9,11-trien-3-one 17-acetate
30. Revalor-h
31. Trenbolone 17
32. A-acetate
33. 17.beta.-hydroxyestra-4,9,11-trien-3-one, Acetate
34. Trenbolone Acetate (usp)
35. Dsstox_cid_26626
36. Dsstox_rid_81775
37. Dsstox_gsid_46626
38. Ru1697
39. Schembl139877
40. Trenbolone Acetate [mi]
41. Chembl1698011
42. Dtxsid2046626
43. Estra-4,9,11-trien-3-one, 17-beta-hydroxy-, Acetate
44. Chebi:192671
45. Estra-4,9,11-trien-3-one, 17-(acetyloxy)-, (17beta)-
46. Trenbolone Acetate [mart.]
47. Bcp11574
48. Trenbolone Acetate [who-dd]
49. Zinc4083873
50. Tox21_112443
51. Bdbm50190646
52. S4795
53. Akos015895158
54. Ccg-267604
55. Cs-3362
56. Db14660
57. Ds-8264
58. Trenbolone Acetate [green Book]
59. Ncgc00167439-03
60. Trenbolone Acetate [usp Impurity]
61. Trenbolone Acetate Ciii [usp-rs]
62. Hy-12360
63. Trenbolone Acetate [usp Monograph]
64. Cas-10161-34-9
65. D06211
66. 161t349
67. Trenbolone-acetate 100 Microg/ml In Acetonitrile
68. Q27288295
69. Trenbolone-acetate. Short Expiry Date Due To Chemical Nature Of Component(s)
70. (8s,13s,14s,17s)-13-methyl-3-oxo-2,3,6,7,8,13,14,15,16,17-decahydro-1h-cyclopenta[a]phenanthren-17-yl Acetate
Molecular Weight | 312.4 g/mol |
---|---|
Molecular Formula | C20H24O3 |
XLogP3 | 2.5 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 2 |
Exact Mass | 312.17254462 g/mol |
Monoisotopic Mass | 312.17254462 g/mol |
Topological Polar Surface Area | 43.4 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 666 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 4 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
Anabolic Agents
These compounds stimulate anabolism and inhibit catabolism. They stimulate the development of muscle mass, strength, and power. (See all compounds classified as Anabolic Agents.)
API Imports and Exports
Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Trenbolone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trenbolone Acetate, including repackagers and relabelers. The FDA regulates Trenbolone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trenbolone Acetate 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 Trenbolone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trenbolone Acetate supplier is an individual or a company that provides Trenbolone Acetate active pharmaceutical ingredient (API) or Trenbolone Acetate finished formulations upon request. The Trenbolone Acetate suppliers may include Trenbolone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Trenbolone Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trenbolone Acetate DMF (Drug Master File) is a document detailing the whole manufacturing process of Trenbolone Acetate active pharmaceutical ingredient (API) in detail. Different forms of Trenbolone Acetate DMFs exist exist since differing nations have different regulations, such as Trenbolone Acetate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trenbolone Acetate DMF submitted to regulatory agencies in the US is known as a USDMF. Trenbolone Acetate USDMF includes data on Trenbolone Acetate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trenbolone Acetate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Trenbolone Acetate suppliers with USDMF 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 Trenbolone Acetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Trenbolone Acetate 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 Trenbolone Acetate 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 Trenbolone Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Trenbolone Acetate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Trenbolone Acetate suppliers with NDC on PharmaCompass.
Trenbolone Acetate 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 Trenbolone Acetate 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 Trenbolone Acetate GMP manufacturer or Trenbolone Acetate GMP API supplier for your needs.
A Trenbolone Acetate CoA (Certificate of Analysis) is a formal document that attests to Trenbolone Acetate's compliance with Trenbolone Acetate specifications and serves as a tool for batch-level quality control.
Trenbolone Acetate CoA mostly includes findings from lab analyses of a specific batch. For each Trenbolone Acetate 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.
Trenbolone Acetate may be tested according to a variety of international standards, such as European Pharmacopoeia (Trenbolone Acetate EP), Trenbolone Acetate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Trenbolone Acetate USP).
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