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1. 2-diethylaminopropiophenone
2. Amfepramon
3. Amfepramone
4. Anorex
5. Delgamer
6. Diethylpropion
7. Dietil Retard
8. Dietil-retard
9. Dietilretard
10. Hydrochloride, Diethylpropion
11. Ifa Norex
12. Lipomin
13. Maruate
14. Modratan
15. Neobes
16. Nobesine
17. Norex, Ifa
18. Phepranon
19. Prfamone
20. Propion
21. Regenon
22. Regibon
23. Tenuate
24. Tepanil
1. Amfepramone Hydrochloride
2. 134-80-5
3. Moderatan
4. Dobesin
5. Tenuate
6. Diethylpropion Hcl
7. Tepanil
8. Anorex
9. Tenuate Dospan
10. Regenon Hydrochloride
11. 2-(diethylamino)propiophenone Hydrochloride
12. Amfepramone (hydrochloride)
13. Prefamone
14. Regenon
15. Amphepramonum Hydrochloride
16. 1-propanone, 2-(diethylamino)-1-phenyl-, Hydrochloride
17. 19v2pl39ng
18. Diethylpropion Hydrochloride Civ
19. Alpha-benzoyltriethylammonium Chloride
20. Alpha-benzoyltriethylamine Hydrochloride
21. D03801
22. Diethylpropion Hydrochloride [usp]
23. Menutil
24. 1-phenyl-2-diethylaminopropanone-1 Hydrochloride
25. Magrex Retard
26. Tenuate-dospan
27. Amfepramon Hydrochloride
28. Lineal-rivo
29. Tepanil Ten-tab
30. Nu-dispoz
31. Dsstox_cid_27816
32. Dsstox_rid_82580
33. Dsstox_gsid_47838
34. Propiophenone, 2-(diethylamino)-, Hydrochloride
35. Diethylpropion Hydrochloride (usp)
36. 2-(diethylamino)-1-phenylpropan-1-one Hydrochloride
37. Cas-134-80-5
38. Chebi:643703
39. 2-diethylaminopropiophenone Hydrochloride
40. Sr-01000220674
41. Ncgc00167475-01
42. Einecs 205-156-5
43. Unii-19v2pl39ng
44. Tenuate (tn)
45. Rac Diethylpropion-d10 Hydrochloride
46. Diethylproion Hydrochloride
47. Cambridge Id 5809497
48. Chembl1693
49. Schembl15483
50. 2-(diethylamino)-1-phenyl-1-propanone Hydrochloride
51. 2-(diethylamino)-1-phenylpropan-1-one;hydrochloride
52. Dtxsid4047838
53. Hy-b0981
54. Tox21_112479
55. Akos015962206
56. Tox21_112479_1
57. Ccg-220122
58. Cs-4472
59. Diethylpropion Hydrochloride [mi]
60. Ncgc00167475-02
61. Ac-16025
62. Amfepramone Hydrochloride [who-dd]
63. As-16865
64. Diethylpropion Hydrochloride [mart.]
65. Diethylpropion Hydrochloride [vandf]
66. Diethylpropion Hydrochloride [usp-rs]
67. .alpha.-benzoyltriethylamine Hydrochloride
68. 090d846
69. Diethylpropion Hydrochloride [orange Book]
70. Diethylpropion Hydrochloride [usp Monograph]
71. Sr-01000220674-1
72. Sr-01000220674-2
73. Q27105182
74. Diethylpropion Hydrochloride Solution, 1.0 Mg/ml In Methanol (with 1% 1 M Hcl; As Free Base), Certified Reference Material
| Molecular Weight | 241.76 g/mol |
|---|---|
| Molecular Formula | C13H20ClNO |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Exact Mass | 241.1233420 g/mol |
| Monoisotopic Mass | 241.1233420 g/mol |
| Topological Polar Surface Area | 20.3 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 193 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
| 1 of 6 | |
|---|---|
| Drug Name | Diethylpropion hydrochloride |
| Active Ingredient | Diethylpropion hydrochloride |
| Dosage Form | Tablet, extended release; Tablet |
| Route | Oral |
| Strength | 75mg; 25mg |
| Market Status | Prescription |
| Company | Lannett Holdings; Corepharma; Avanthi |
| 2 of 6 | |
|---|---|
| Drug Name | Tenuate |
| Active Ingredient | Diethylpropion hydrochloride |
| Dosage Form | Tablet |
| Route | Oral |
| Strength | 25mg |
| Market Status | Prescription |
| Company | Watson Pharms |
| 3 of 6 | |
|---|---|
| Drug Name | Tenuate dospan |
| PubMed Health | Diethylpropion (By mouth) |
| Drug Classes | Appetite Suppressant, Centrally Acting |
| Drug Label | Diethylpropion hydrochloride, USPis available for oral administration in immediate-release tablets containing 25 mg diethylpropion hydrochloride. The inactive ingredients in each immediate-release tablet are: corn starch, lactose monohydrate, magne... |
| Active Ingredient | Diethylpropion hydrochloride |
| Dosage Form | Tablet, extended release |
| Route | Oral |
| Strength | 75mg |
| Market Status | Prescription |
| Company | Watson Pharms |
| 4 of 6 | |
|---|---|
| Drug Name | Diethylpropion hydrochloride |
| Active Ingredient | Diethylpropion hydrochloride |
| Dosage Form | Tablet, extended release; Tablet |
| Route | Oral |
| Strength | 75mg; 25mg |
| Market Status | Prescription |
| Company | Lannett Holdings; Corepharma; Avanthi |
| 5 of 6 | |
|---|---|
| Drug Name | Tenuate |
| Active Ingredient | Diethylpropion hydrochloride |
| Dosage Form | Tablet |
| Route | Oral |
| Strength | 25mg |
| Market Status | Prescription |
| Company | Watson Pharms |
| 6 of 6 | |
|---|---|
| Drug Name | Tenuate dospan |
| PubMed Health | Diethylpropion (By mouth) |
| Drug Classes | Appetite Suppressant, Centrally Acting |
| Drug Label | Diethylpropion hydrochloride, USPis available for oral administration in immediate-release tablets containing 25 mg diethylpropion hydrochloride. The inactive ingredients in each immediate-release tablet are: corn starch, lactose monohydrate, magne... |
| Active Ingredient | Diethylpropion hydrochloride |
| Dosage Form | Tablet, extended release |
| Route | Oral |
| Strength | 75mg |
| Market Status | Prescription |
| Company | Watson Pharms |
Appetite Depressants
Agents that are used to suppress appetite. (See all compounds classified as Appetite Depressants.)
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FDF Dossiers
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DOSAGE - TABLET;ORAL - 25MG **Federal Registe...DOSAGE - TABLET;ORAL - 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 11722
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 75MG...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 12546
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PharmaCompass offers a list of Diethylpropion Hydrochloride 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 Diethylpropion Hydrochloride manufacturer or Diethylpropion Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diethylpropion Hydrochloride manufacturer or Diethylpropion Hydrochloride supplier.
PharmaCompass also assists you with knowing the Diethylpropion Hydrochloride API Price utilized in the formulation of products. Diethylpropion Hydrochloride API Price is not always fixed or binding as the Diethylpropion Hydrochloride Price is obtained through a variety of data sources. The Diethylpropion Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Amfepramon hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amfepramon hydrochloride, including repackagers and relabelers. The FDA regulates Amfepramon hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amfepramon hydrochloride 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 Amfepramon hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amfepramon hydrochloride supplier is an individual or a company that provides Amfepramon hydrochloride active pharmaceutical ingredient (API) or Amfepramon hydrochloride finished formulations upon request. The Amfepramon hydrochloride suppliers may include Amfepramon hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Amfepramon hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Amfepramon hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Amfepramon hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Amfepramon hydrochloride DMFs exist exist since differing nations have different regulations, such as Amfepramon hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Amfepramon hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Amfepramon hydrochloride USDMF includes data on Amfepramon hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Amfepramon hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Amfepramon hydrochloride suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Amfepramon hydrochloride Drug Master File in Korea (Amfepramon hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Amfepramon hydrochloride. The MFDS reviews the Amfepramon hydrochloride KDMF as part of the drug registration process and uses the information provided in the Amfepramon hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Amfepramon hydrochloride KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Amfepramon hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Amfepramon hydrochloride suppliers with KDMF 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 Amfepramon hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Amfepramon hydrochloride 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 Amfepramon hydrochloride 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 Amfepramon hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Amfepramon hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Amfepramon hydrochloride suppliers with NDC on PharmaCompass.
Amfepramon hydrochloride 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 Amfepramon hydrochloride 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 Amfepramon hydrochloride GMP manufacturer or Amfepramon hydrochloride GMP API supplier for your needs.
A Amfepramon hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Amfepramon hydrochloride's compliance with Amfepramon hydrochloride specifications and serves as a tool for batch-level quality control.
Amfepramon hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Amfepramon hydrochloride 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.
Amfepramon hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Amfepramon hydrochloride EP), Amfepramon hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Amfepramon hydrochloride USP).
