Synopsis
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1. Hydrochloride, Promazine
2. Promazine
3. Protactyl
4. Sinophenin
5. Sparine
1. 53-60-1
2. Promazine Hcl
3. Sparine
4. Starazin
5. Talofen
6. Promazine (hydrochloride)
7. Promazine Monohydrochloride
8. Rp 4560
9. N,n-dimethyl-3-(10h-phenothiazin-10-yl)propan-1-amine Hydrochloride
10. Nsc-17468
11. Promazinehydrochloride
12. Promazine Hydrochloride [usp]
13. Mls000069671
14. U16eor79u4
15. 10-(3-(dimethylamino)propyl)phenothiazine Monohydrochloride
16. 10h-phenothiazine-10-propanamine, N,n-dimethyl-, Monohydrochloride
17. N-(3-(dimethylamino)propyl)phenothiazine Hydrochloride
18. 10-(3-(dimethylamino)propyl)phenothiazine Hydrochloride
19. Smr000058499
20. Dsstox_cid_26949
21. Dsstox_rid_82026
22. Dsstox_gsid_46949
23. 10-(gamma-dimethylamino-n-propyl)phenothiazine Hydrochloride
24. Promazine Hydrochloride (usp)
25. Chebi:8460
26. N,n-dimethyl-3-phenothiazin-10-ylpropan-1-amine;hydrochloride
27. Chlorowodorek Promazyny
28. Chlorowodorek Promazyny [polish]
29. Cas-53-60-1
30. Sr-01000000228
31. Ncgc00015829-02
32. Einecs 200-179-7
33. Nsc 17468
34. N-[3-(dimethylamino)propyl]phenothiazine Hydrochloride
35. 10-(3-[dimethylamino]propyl)phenothiazine Hydrochloride
36. 10-[3-(dimethylamino)propyl]phenothiazine Hydrochloride
37. Unii-u16eor79u4
38. Esparinal
39. Verofen
40. Ai3-28022
41. Sr-01000000228-4
42. Promazine Chloride
43. Promazine-d6 Hcl
44. Prestwick_974
45. Sparine (tn)
46. Romtiazin Hydrochloride
47. Opera_id_41
48. Sinophenin Hydrochloride
49. Phenothiazine, 10-(3-(dimethylamino)propyl)-, Hydrochloride
50. Propazin (pharmaceutical)
51. Regid_for_cid_5887
52. Mls001148436
53. Mls002222285
54. Schembl123418
55. Spectrum1500509
56. 10-(3-dimethylaminopropyl)phenothiazine Hydrochloride
57. Chembl1200469
58. Dtxsid4046949
59. Hms1570k07
60. Hms1920l14
61. Pharmakon1600-01500509
62. Hy-b1225
63. Nsc17468
64. Phenothiazine, 10-(3-(dimethylamino)propyl)-, Monohydrochloride
65. Promazine Hydrochloride [mi]
66. Tox21_110235
67. Tox21_500961
68. 10-h-phenothiazine-10-propanamine, N,n-dimethyl-, Monohydrochloride
69. Ccg-40284
70. Nsc757300
71. S5428
72. Akos015964305
73. Tox21_110235_1
74. Cs-4873
75. Ks-1384
76. Lp00961
77. Nsc-757300
78. Promazine Hydrochloride [mart.]
79. Promazine Hydrochloride [vandf]
80. Promazine Hydrochloride [usp-rs]
81. Promazine Hydrochloride [who-dd]
82. Ncgc00015829-12
83. Ncgc00094262-01
84. Ncgc00094262-02
85. Ncgc00094262-03
86. Ncgc00094262-04
87. Ncgc00094262-05
88. Ncgc00261646-01
89. Ac-18101
90. Promazine Hydrochloride [green Book]
91. Eu-0100961
92. Ft-0674047
93. Promazine Hydrochloride [orange Book]
94. Promazine Hydrochloride [ep Monograph]
95. Wln: T C666 Bn Isj B3n1&1 &gh
96. D00797
97. D78322
98. P 6656
99. Promazine Hydrochloride [usp Monograph]
100. Sr-01000000228-2
101. Sr-01000000228-8
102. W-105721
103. Q27108085
104. Z2784093694
105. Promazine Hydrochloride, Vetranal(tm), Analytical Standard
106. 10-(.gamma.-dimethylamino-n-propyl)phenothiazine Hydrochloride
107. Dimethyl[3-(10h-phenothiazin-10-yl)propyl]amine Hydrochloride
108. Promazine Hydrochloride 1.0 Mg/ml In Methanol (as Free Base)
109. 10h-phenothiazine-10-propanamine, N,n-dimethyl-, Hydrochloride (1:1)
110. N,n-dimethyl-3-(10h-phenothiazin-10-yl)-1-propanamine Hydrochloride
111. Promazine Hydrochloride, European Pharmacopoeia (ep) Reference Standard
112. Promazine Hydrochloride, United States Pharmacopeia (usp) Reference Standard
| Molecular Weight | 320.9 g/mol |
|---|---|
| Molecular Formula | C17H21ClN2S |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 4 |
| Exact Mass | 320.1113975 g/mol |
| Monoisotopic Mass | 320.1113975 g/mol |
| Topological Polar Surface Area | 31.8 Ų |
| Heavy Atom Count | 21 |
| Formal Charge | 0 |
| Complexity | 285 |
| 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 | 2 |
Antiemetics
Drugs used to prevent NAUSEA or VOMITING. (See all compounds classified as Antiemetics.)
Dopamine Antagonists
Drugs that bind to but do not activate DOPAMINE RECEPTORS, thereby blocking the actions of dopamine or exogenous agonists. Many drugs used in the treatment of psychotic disorders (ANTIPSYCHOTIC AGENTS) are dopamine antagonists, although their therapeutic effects may be due to long-term adjustments of the brain rather than to the acute effects of blocking dopamine receptors. Dopamine antagonists have been used for several other clinical purposes including as ANTIEMETICS, in the treatment of Tourette syndrome, and for hiccup. Dopamine receptor blockade is associated with NEUROLEPTIC MALIGNANT SYNDROME. (See all compounds classified as Dopamine Antagonists.)
Antipsychotic Agents
Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus. (See all compounds classified as Antipsychotic Agents.)
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ABOUT THIS PAGE
43
PharmaCompass offers a list of Promazine 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 Promazine manufacturer or Promazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Promazine manufacturer or Promazine supplier.
PharmaCompass also assists you with knowing the Promazine API Price utilized in the formulation of products. Promazine API Price is not always fixed or binding as the Promazine Price is obtained through a variety of data sources. The Promazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Talofen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Talofen, including repackagers and relabelers. The FDA regulates Talofen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Talofen 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 Talofen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Talofen supplier is an individual or a company that provides Talofen active pharmaceutical ingredient (API) or Talofen finished formulations upon request. The Talofen suppliers may include Talofen API manufacturers, exporters, distributors and traders.
click here to find a list of Talofen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Talofen DMF (Drug Master File) is a document detailing the whole manufacturing process of Talofen active pharmaceutical ingredient (API) in detail. Different forms of Talofen DMFs exist exist since differing nations have different regulations, such as Talofen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Talofen DMF submitted to regulatory agencies in the US is known as a USDMF. Talofen USDMF includes data on Talofen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Talofen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Talofen suppliers with USDMF on PharmaCompass.
A Talofen CEP of the European Pharmacopoeia monograph is often referred to as a Talofen Certificate of Suitability (COS). The purpose of a Talofen CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Talofen EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Talofen to their clients by showing that a Talofen CEP has been issued for it. The manufacturer submits a Talofen CEP (COS) as part of the market authorization procedure, and it takes on the role of a Talofen CEP holder for the record. Additionally, the data presented in the Talofen CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Talofen DMF.
A Talofen CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Talofen CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Talofen suppliers with CEP (COS) on PharmaCompass.
Talofen 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 Talofen 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 Talofen GMP manufacturer or Talofen GMP API supplier for your needs.
A Talofen CoA (Certificate of Analysis) is a formal document that attests to Talofen's compliance with Talofen specifications and serves as a tool for batch-level quality control.
Talofen CoA mostly includes findings from lab analyses of a specific batch. For each Talofen 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.
Talofen may be tested according to a variety of international standards, such as European Pharmacopoeia (Talofen EP), Talofen JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Talofen USP).
