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1. Estra-1,3,5(10)-trien-17-one, 3-(sulfooxy)-, Compd. With Piperazine (1:1)
2. Genoral
3. Harmogen
4. Harmonet
5. Ogen
6. Ortho-est
7. Piperazine Estrone Sulfate
1. 7280-37-7
2. Piperazine Estrone Sulfate
3. Ogen
4. Harmogen
5. Ortho-est
6. Estrone Sulfate Piperazine Salt
7. Sulestrex Piperazine
8. Piperazine Estrone Sulphate
9. Estra-1,3,5(10)-trien-17-one, 3-(sulfooxy)-, Compd. With Piperazine (1:1)
10. Svi38uy019
11. Piperazine Estronesulfate
12. Nsc-758912
13. Estrone Hydrogen Sulfate Compound With Piperazine (1:1)
14. Sulestrex
15. Unii-svi38uy019
16. Piperazine (8r,9s,13s,14s)-13-methyl-17-oxo-7,8,9,11,12,13,14,15,16,17-decahydro-6h-cyclopenta[a]phenanthren-3-yl Sulfate
17. Ogen 5
18. Pipestrone
19. Estropipate [usp:inn:ban]
20. Ogen 2.5
21. Ogen .625
22. Ogen 1.25
23. Einecs 230-696-3
24. Estropipate (usp)
25. Ogen (tn)
26. Piperazineestronesulfate
27. Ncgc00016682-02
28. Dsstox_cid_3005
29. Cas-7280-37-7
30. Estropipate [vandf]
31. Piperazine Oestrone Sulphate
32. Conjugated Estrogens: Piperazine Estrone Sulfate
33. Dsstox_rid_76828
34. Estropipate [mart.]
35. Dsstox_gsid_23005
36. Schembl21577
37. Estropipate [usp-rs]
38. Estropipate [who-dd]
39. Mls002153957
40. Chebi:4873
41. Chembl1200980
42. Dtxsid3023005
43. Piperazine, Compd. With Estrone Hydrogen Sulfate (1:1)
44. Estrone, Hydrogen Sulfate, Compd. With Piperazine (1:1)
45. Estropipate [orange Book]
46. Hms1570i17
47. Hms2097i17
48. Hms2232o19
49. Hms3714i17
50. Estropipate [usp Monograph]
51. Bcp05424
52. Hy-b1361
53. Tox21_113350
54. S5288
55. Akos024457702
56. Estra-1,3,5(10)-trien-17-one 3-sulphate, Compound With Piperazine (1:1)
57. Piperazine, Compd. With 3-(sulfooxy)estra-1,3,5(10)-trien-17-one (1:1)
58. Bcp9000662
59. Ccg-220688
60. Cs-4818
61. Estropipate, >=98% (hplc), Powder
62. Nsc 758912
63. [(8r,9s,13s,14s)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-3-yl] Hydrogen Sulfate,piperazine
64. Smr001233296
65. Am20080957
66. Estrone Sulfate Piperazine Salt [mi]
67. D00948
68. 280e377
69. A837628
70. Sr-01000000235
71. Q5401860
72. Sr-01000000235-5
73. Estrone Hydrogen Sulphate Compound With Piperazine (1:1)
74. Estropipate, United States Pharmacopeia (usp) Reference Standard
75. 17-oxoestra-1,3,5(10)-trien-3-yl Hydrogen Sulfate - Piperazine (1:1)
76. [(8r,9s,13s,14s)-13-methyl-17-oxidanylidene-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-3-yl] Hydrogen Sulfate; Piperazine
77. [(8r,9s,13s,14s)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-3-yl] Hydrogen Sulfate;piperazine
78. Piperazine; Sulfuric Acid [(8r,9s,13s,14s)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthren-3-yl] Ester
Molecular Weight | 436.6 g/mol |
---|---|
Molecular Formula | C22H32N2O5S |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 7 |
Rotatable Bond Count | 2 |
Exact Mass | 436.20319330 g/mol |
Monoisotopic Mass | 436.20319330 g/mol |
Topological Polar Surface Area | 113 Ų |
Heavy Atom Count | 30 |
Formal Charge | 0 |
Complexity | 650 |
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 | 2 |
1 of 10 | |
---|---|
Drug Name | Estropipate |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 1.5mg; 3mg; 0.75mg |
Market Status | Prescription |
Company | Watson Labs; Mylan; Barr |
2 of 10 | |
---|---|
Drug Name | Ogen .625 |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 0.75mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
3 of 10 | |
---|---|
Drug Name | Ogen 1.25 |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 1.5mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
4 of 10 | |
---|---|
Drug Name | Ogen 2.5 |
PubMed Health | Estropipate |
Drug Classes | Endocrine-Metabolic Agent, Female Reproductive Agent, Musculoskeletal Agent |
Drug Label | Estropipate (formerly piperazine estrone sulfate), is a natural estrogenic substance prepared from purified crystalline estrone, solubilized as the sulfate and stabilized with piperazine. It is appreciably soluble in water and has almost no odor or t... |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 3mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
5 of 10 | |
---|---|
Drug Name | Ogen 5 |
PubMed Health | Estrogen |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 6mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
6 of 10 | |
---|---|
Drug Name | Estropipate |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 1.5mg; 3mg; 0.75mg |
Market Status | Prescription |
Company | Watson Labs; Mylan; Barr |
7 of 10 | |
---|---|
Drug Name | Ogen .625 |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 0.75mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
8 of 10 | |
---|---|
Drug Name | Ogen 1.25 |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 1.5mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
9 of 10 | |
---|---|
Drug Name | Ogen 2.5 |
PubMed Health | Estropipate |
Drug Classes | Endocrine-Metabolic Agent, Female Reproductive Agent, Musculoskeletal Agent |
Drug Label | Estropipate (formerly piperazine estrone sulfate), is a natural estrogenic substance prepared from purified crystalline estrone, solubilized as the sulfate and stabilized with piperazine. It is appreciably soluble in water and has almost no odor or t... |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 3mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
10 of 10 | |
---|---|
Drug Name | Ogen 5 |
PubMed Health | Estrogen |
Active Ingredient | Estropipate |
Dosage Form | Tablet |
Route | Oral |
Strength | 6mg |
Market Status | Prescription |
Company | Pharmacia And Upjohn |
Contraceptive Agents, Hormonal
Contraceptive agents that act on the ENDOCRINE SYSTEM. (See all compounds classified as Contraceptive Agents, Hormonal.)
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PharmaCompass offers a list of Estropipate 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 Estropipate manufacturer or Estropipate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Estropipate manufacturer or Estropipate supplier.
PharmaCompass also assists you with knowing the Estropipate API Price utilized in the formulation of products. Estropipate API Price is not always fixed or binding as the Estropipate Price is obtained through a variety of data sources. The Estropipate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DSSTox_CID_3005 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3005, including repackagers and relabelers. The FDA regulates DSSTox_CID_3005 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3005 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A DSSTox_CID_3005 supplier is an individual or a company that provides DSSTox_CID_3005 active pharmaceutical ingredient (API) or DSSTox_CID_3005 finished formulations upon request. The DSSTox_CID_3005 suppliers may include DSSTox_CID_3005 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_3005 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSSTox_CID_3005 DMF (Drug Master File) is a document detailing the whole manufacturing process of DSSTox_CID_3005 active pharmaceutical ingredient (API) in detail. Different forms of DSSTox_CID_3005 DMFs exist exist since differing nations have different regulations, such as DSSTox_CID_3005 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DSSTox_CID_3005 DMF submitted to regulatory agencies in the US is known as a USDMF. DSSTox_CID_3005 USDMF includes data on DSSTox_CID_3005's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DSSTox_CID_3005 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DSSTox_CID_3005 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 DSSTox_CID_3005 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for DSSTox_CID_3005 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 DSSTox_CID_3005 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 DSSTox_CID_3005 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a DSSTox_CID_3005 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of DSSTox_CID_3005 suppliers with NDC on PharmaCompass.
DSSTox_CID_3005 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 DSSTox_CID_3005 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 DSSTox_CID_3005 GMP manufacturer or DSSTox_CID_3005 GMP API supplier for your needs.
A DSSTox_CID_3005 CoA (Certificate of Analysis) is a formal document that attests to DSSTox_CID_3005's compliance with DSSTox_CID_3005 specifications and serves as a tool for batch-level quality control.
DSSTox_CID_3005 CoA mostly includes findings from lab analyses of a specific batch. For each DSSTox_CID_3005 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.
DSSTox_CID_3005 may be tested according to a variety of international standards, such as European Pharmacopoeia (DSSTox_CID_3005 EP), DSSTox_CID_3005 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DSSTox_CID_3005 USP).