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Chemistry

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Also known as: Ketoconazole, (+)-ketoconazole, 65277-42-1, (2r,4s)-ketoconazole, 142128-59-4, Kuric
Molecular Formula
C26H28Cl2N4O4
Molecular Weight
531.4  g/mol
InChI Key
XMAYWYJOQHXEEK-OZXSUGGESA-N

Ketoconazole
Broad spectrum antifungal agent used for long periods at high doses, especially in immunosuppressed patients.
1 2D Structure

Ketoconazole

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
1-[4-[4-[[(2R,4S)-2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]ethanone
2.1.2 InChI
InChI=1S/C26H28Cl2N4O4/c1-19(33)31-10-12-32(13-11-31)21-3-5-22(6-4-21)34-15-23-16-35-26(36-23,17-30-9-8-29-18-30)24-7-2-20(27)14-25(24)28/h2-9,14,18,23H,10-13,15-17H2,1H3/t23-,26-/m0/s1
2.1.3 InChI Key
XMAYWYJOQHXEEK-OZXSUGGESA-N
2.1.4 Canonical SMILES
CC(=O)N1CCN(CC1)C2=CC=C(C=C2)OCC3COC(O3)(CN4C=CN=C4)C5=C(C=C(C=C5)Cl)Cl
2.1.5 Isomeric SMILES
CC(=O)N1CCN(CC1)C2=CC=C(C=C2)OC[C@H]3CO[C@](O3)(CN4C=CN=C4)C5=C(C=C(C=C5)Cl)Cl
2.2 Synonyms
2.2.1 MeSH Synonyms

1. Ketoconazole

2. Nizoral

3. R 41400

4. R-41400

5. R41,400

6. R41400

2.2.2 Depositor-Supplied Synonyms

1. Ketoconazole

2. (+)-ketoconazole

3. 65277-42-1

4. (2r,4s)-ketoconazole

5. 142128-59-4

6. Kuric

7. Ketocanazole

8. Cpd000058460

9. Chembl75

10. Smr000058460

11. Mls000069784

12. Mls001146934

13. 1-[4-[4-[[(2r,4s)-2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]ethanone

14. 1-acetyl-4-(4-{[(2r,4s)-2-(2,4-dichlorophenyl)-2-(1h-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy}phenyl)piperazine

15. Chebi:48336

16. Dsstox_cid_9879

17. R-41400

18. Dsstox_rid_78829

19. Dsstox_gsid_29879

20. 1-(4-(4-(((2r,4s)-2-((1h-imidazol-1-yl)methyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl)methoxy)phenyl)piperazin-1-yl)ethanone

21. Mfcd00058579

22. Rac-trans-ketoconazole

23. Ktz

24. Sr-01000075626

25. Sr-01000597381

26. Ketoconazole (k)

27. (+)-ketoconazol

28. Ketoconazole,(s)

29. Ncgc00016907-01

30. Prestwick_744

31. Cas-65277-42-1

32. Tocris-1103

33. Opera_id_397

34. Prestwick0_000389

35. Prestwick1_000389

36. Prestwick2_000389

37. Prestwick3_000389

38. R 41,400

39. Upcmld-dp138

40. Schembl8407

41. Lopac0_000666

42. Bspbio_000577

43. Mls000758224

44. Mls001423987

45. Mls002207053

46. Mls002222255

47. Bidd:gt0696

48. Us9150527, Ketoconazole

49. Spbio_002498

50. Amy917

51. Bdbm8610

52. Bpbio1_000635

53. Dtxsid7029879

54. Upcmld-dp138:001

55. Bdbm60666

56. Hy-b0105a

57. Ketoconazole, >=98% (hplc)

58. Dtxsid901316748

59. Hms1569m19

60. Hms2051a19

61. Hms2089n05

62. Hms2096m19

63. Hms2234h17

64. Hms3262e13

65. Hms3414j19

66. Hms3678j17

67. Hms3713m19

68. Zinc643138

69. Bcp28528

70. Piperazine, (+/-)-1-acetyl-4-[4-[[(2r,4s)-2-(2,4-dichlorophenyl)-2-(1h-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-, Rel-

71. Ketoconazole 2.0 Mg/ml In Methanol

72. Tox21_110676

73. Tox21_300267

74. Tox21_500666

75. Ei-107

76. S1353

77. Akos007930650

78. Ccg-100815

79. Cs-1846

80. Ks-1205

81. Lp00666

82. Nc00065

83. Sdccgsbi-0050645.p002

84. Ketoconazole 100 Microg/ml In Methanol

85. Mrf-0000100

86. 24f2-1,25(oh)d3

87. Ncgc00025000-01

88. Ncgc00025000-02

89. Ncgc00025000-03

90. Ncgc00025000-04

91. Ncgc00025000-05

92. Ncgc00025000-06

93. Ncgc00025000-07

94. Ncgc00025000-08

95. Ncgc00025000-09

96. Ncgc00025000-10

97. Ncgc00025000-14

98. Ncgc00025000-16

99. Ncgc00025000-28

100. Ncgc00253967-01

101. Ncgc00261351-01

102. ( Inverted Exclamation Marka)-ketoconazol

103. (+/-)-cis-1-acetyl-4-[4-[[2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazine

104. Ac-15957

105. Cis-1-acetyl-4-[4-[[2-(2,4-

106. 3-dioxolan-4-yl)-methoxy]phenyl)piperazine

107. Ketoconazole 100 Microg/ml In Acetonitrile

108. Eu-0100666

109. K0045

110. Sw196888-4

111. Bim-0050645.0001

112. K 1003

113. M02048

114. 277k421

115. Ketoconazole, Antibiotic For Culture Media Use Only

116. Q-201267

117. Sr-01000075626-1

118. Sr-01000075626-4

119. Sr-01000597381-1

120. Sr-01000597381-6

121. Brd-k29113274-001-03-6

122. Brd-k29113274-001-11-9

123. Brd-k29113274-001-21-8

124. Q27121163

125. (+)-r 41400

126. Ketoconazole, British Pharmacopoeia (bp) Reference Standard

127. Ketoconazole, European Pharmacopoeia (ep) Reference Standard

128. Ketoconazole, United States Pharmacopeia (usp) Reference Standard

129. Dichlorophenyl)-2-(1h-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-piperazine

130. Ketoconazole, Pharmaceutical Secondary Standard; Certified Reference Material

131. (2r,4s)-1-acetyl-4-(4-{[2-(2,4-dichlorophenyl)-2-(1h-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy}phenyl)piperazine

132. 1-(4-(4-(((2r,4s)-2-((1h-imidazol-1-yl)methyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl)methoxy)phenyl)piperazin-1-yl)ethan-1-one

133. Cis-1-acetyl-4-[4-[[2-(2,4-dichlorophenyl)-2-(1h-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl] Methoxy]phenyl]piperazine

134. Kz

135. Piperazine, (+)-1-acetyl-4-[4-[[2-(2,4-dichlorophenyl)-2-(1h-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-

2.3 Create Date
2005-08-01
3 Chemical and Physical Properties
Molecular Weight 531.4 g/mol
Molecular Formula C26H28Cl2N4O4
XLogP34.3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count6
Rotatable Bond Count7
Exact Mass530.1487608 g/mol
Monoisotopic Mass530.1487608 g/mol
Topological Polar Surface Area69.1 Ų
Heavy Atom Count36
Formal Charge0
Complexity735
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Drug and Medication Information
4.1 Drug Information
1 of 10  
Drug NameExtina
PubMed HealthKetoconazole
Drug LabelEXTINA Foam contains 2% ketoconazole USP, an antifungal agent, in a thermolabile hydroethanolic foam for topical application.The chemical name for ketoconazole is piperazine, 1-acetyl-4-[4-[[2-(2,4-dichlorophenyl) -2-(1H-imidazol-l-ylmethyl)-1,3-di...
Active IngredientKetoconazole
Dosage FormAerosol, foam
RouteTopical
Strength2%
Market StatusPrescription
CompanyDelcor Abet

2 of 10  
Drug NameKetoconazole
PubMed HealthKetoconazole
Drug LabelNIZORAL is a synthetic broad-spectrum antifungal agent available in scored white tablets, each containing 200 mg ketoconazole base for oral administration. Inactive ingredients are colloidal silicon dioxide, corn starch, lactose, magnesium stearate...
Active IngredientKetoconazole
Dosage FormShampoo; Tablet; Cream; Aerosol, foam
RouteOral; Topical
Strength200mg; 2%
Market StatusPrescription
CompanyTeva; Taro; Fougera Pharms; Perrigo New York; Tolmar; Mylan; Perrigo Israel

3 of 10  
Drug NameNizoral
PubMed HealthKetoconazole
Drug LabelNIZORAL is a synthetic broad-spectrum antifungal agent available in scored white tablets, each containing 200 mg ketoconazole base for oral administration. Inactive ingredients are colloidal silicon dioxide, corn starch, lactose, magnesium stearate...
Active IngredientKetoconazole
Dosage FormShampoo
RouteTopical
Strength2%
Market StatusPrescription
CompanyJanben Pharms

4 of 10  
Drug NameNizoral a-d
PubMed HealthKetoconazole (On the skin)
Active IngredientKetoconazole
Dosage FormShampoo
RouteTopical
Strength1%
Market StatusOver the Counter
CompanyMcneil Cons

5 of 10  
Drug NameXolegel
PubMed HealthKetoconazole
Drug LabelXOLEGEL contains the antifungal agent ketoconazole USP at 2% in a topical anhydrous gel vehicle for topical administration.Chemically, ketoconazole is ()-cis-1-Acetyl-4-[p-[[2-(2,4-dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methox...
Active IngredientKetoconazole
Dosage FormGel
RouteTopical
Strength2%
Market StatusPrescription
CompanyAqua Pharms

6 of 10  
Drug NameExtina
PubMed HealthKetoconazole
Drug LabelEXTINA Foam contains 2% ketoconazole USP, an antifungal agent, in a thermolabile hydroethanolic foam for topical application.The chemical name for ketoconazole is piperazine, 1-acetyl-4-[4-[[2-(2,4-dichlorophenyl) -2-(1H-imidazol-l-ylmethyl)-1,3-di...
Active IngredientKetoconazole
Dosage FormAerosol, foam
RouteTopical
Strength2%
Market StatusPrescription
CompanyDelcor Abet

7 of 10  
Drug NameKetoconazole
PubMed HealthKetoconazole
Drug LabelNIZORAL is a synthetic broad-spectrum antifungal agent available in scored white tablets, each containing 200 mg ketoconazole base for oral administration. Inactive ingredients are colloidal silicon dioxide, corn starch, lactose, magnesium stearate...
Active IngredientKetoconazole
Dosage FormShampoo; Tablet; Cream; Aerosol, foam
RouteOral; Topical
Strength200mg; 2%
Market StatusPrescription
CompanyTeva; Taro; Fougera Pharms; Perrigo New York; Tolmar; Mylan; Perrigo Israel

8 of 10  
Drug NameNizoral
PubMed HealthKetoconazole
Drug LabelNIZORAL is a synthetic broad-spectrum antifungal agent available in scored white tablets, each containing 200 mg ketoconazole base for oral administration. Inactive ingredients are colloidal silicon dioxide, corn starch, lactose, magnesium stearate...
Active IngredientKetoconazole
Dosage FormShampoo
RouteTopical
Strength2%
Market StatusPrescription
CompanyJanben Pharms

9 of 10  
Drug NameNizoral a-d
PubMed HealthKetoconazole (On the skin)
Active IngredientKetoconazole
Dosage FormShampoo
RouteTopical
Strength1%
Market StatusOver the Counter
CompanyMcneil Cons

10 of 10  
Drug NameXolegel
PubMed HealthKetoconazole
Drug LabelXOLEGEL contains the antifungal agent ketoconazole USP at 2% in a topical anhydrous gel vehicle for topical administration.Chemically, ketoconazole is ()-cis-1-Acetyl-4-[p-[[2-(2,4-dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methox...
Active IngredientKetoconazole
Dosage FormGel
RouteTopical
Strength2%
Market StatusPrescription
CompanyAqua Pharms

4.2 Therapeutic Uses

Antifungal agents

National Library of Medicine's Medical Subject Headings. Ketoconazole. Online file (MeSH, 2014). Available from, as of August 28, 2014: https://www.nlm.nih.gov/mesh/2014/mesh_browser/MBrowser.html


Nizoral Tablets should be used only when other effective antifungal therapy is not available or tolerated and the potential benefits are considered to outweigh the potential risks. Nizoral (ketoconazole) Tablets are indicated for the treatment of the following systemic fungal infections in patients who have failed or who are intolerant to other therapies: blastomycosis, coccidioidomycosis, histoplasmosis, chromomycosis, and paracoccidioidomycosis. Nizoral Tablets should not be used for fungal meningitis because it penetrates poorly into the cerebrospinal fluid. /Included in US product label/

NIH; DailyMed. Current Medication Information for Nizoral (Ketoconazole) Tablet (Revised: March 2014). Available from, as of November 11, 2014: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=090660c1-6e6d-457f-adb5-046ddfcd1465


Oral ketoconazole has been used for the palliative treatment of Cushing's syndrome (hypercortisolism), including adrenocortical hyperfunction associated with adrenal or pituitary adenoma or ectopic corticotropin-secreting tumors. Based on ketoconazole's endocrine effects, the drug has been used in the treatment of advanced prostatic carcinoma. Safety and efficacy of ketoconazole have not been established for either of these indications. Oral ketoconazole also has been used in the treatment of hypercalcemia in patients with sarcoidosis and the treatment of tuberculosis-associated hypercalcemia and idiopathic infantile hypercalcemia and hypercalciuria. /NOT included in US product label/

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014


Ketoconazole has been used for the treatment of sporotrichosis caused by Sporothrix schenckii; however, the drug is not recommended since it is less effective and associated with more adverse effects than some other azoles. Oral itraconazole is considered the drug of choice for the treatment of cutaneous, lymphocutaneous, or mild pulmonary or osteoarticular sporotrichosis and for follow-up therapy in more severe infections after a response has been obtained with IV amphotericin B. /NOT included in US product label/

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014


For more Therapeutic Uses (Complete) data for KETOCONAZOLE (18 total), please visit the HSDB record page.


4.3 Drug Warning

/BOXED WARNING/ WARNING. Nizoral Tablets should be used only when other effective antifungal therapy is not available or tolerated and the potential benefits are considered to outweigh the potential risks. Hepatotoxicity: Serious hepatotoxicity, including cases with a fatal outcome or requiring liver transplantation has occurred with the use of oral ketoconazole. Some patients had no obvious risk factors for liver disease. Patients receiving this drug should be informed by the physician of the risk and should be closely monitored. QT Prolongation and Drug Interactions Leading to QT Prolongation: Co-administration of the following drugs with ketoconazole is contraindicated: dofetilide, quinidine, pimozide, cisapride, methadone, disopyramide, dronedarone, ranolazine. Ketoconazole can cause elevated plasma concentrations of these drugs and may prolong QT intervals, sometimes resulting in life-threatening ventricular dysrhythmias such as torsades de pointes.

NIH; DailyMed. Current Medication Information for Nizoral (Ketoconazole) Tablet (Revised: March 2014). Available from, as of November 11, 2014: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=090660c1-6e6d-457f-adb5-046ddfcd1465


Transient increases in serum AST, ALT, and alkaline phosphatase concentrations may occur during ketoconazole therapy. Serious hepatotoxicity has occurred in patients receiving oral ketoconazole, including cases that were fatal or required liver transplantation. Hepatotoxicity may be hepatocellular (in most cases), cholestatic, or a mixed pattern of injury. Although ketoconazole-induced hepatotoxicity usually is reversible following discontinuance of the drug, recovery may take several months and rarely death has occurred. Symptomatic hepatotoxicity usually is apparent within the first few months of ketoconazole therapy, but occasionally may be apparent within the first week of therapy. Some patients with ketoconazole-induced hepatotoxicity had no obvious risk factors for liver disease. Serious hepatotoxicity has been reported in patients receiving high oral ketoconazole dosage for short treatment durations and in patients receiving low oral dosage of the drug for long durations. Many of the reported cases of hepatotoxicity occurred in patients who received the drug for the treatment of tinea unguium (onychomycosi or the treatment of chronic, refractory dermatophytoses. Ketoconazole-induced hepatitis has been reported in some children.

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014, p. 521


Coadministration of a number of CYP3A4 substrates such as dofetilide, quinidine cisapride and pimozide is contraindicated with Nizoral Tablets. Coadministration with ketoconazole can cause elevated plasma concentrations of these drugs and may increase or prolong both therapeutic and adverse effects to such an extent that a potentially serious adverse reaction may occur. For example, increased plasma concentrations of some of these drugs can lead to QT prolongation and sometimes resulting in life-threatening ventricular tachyarrhythmias including occurrences of torsades de pointes, a potentially fatal arrhythmia. Additionally, the following other drugs are contraindicated with Nizoral Tablets: methadone, disopyramide, dronedarone, ergot alkaloids such as dihydroergotamine, ergometrine, ergotamine, methylergometrine, irinotecan, lurasidone, oral midazolam, alprazolam, triazolam, felodipine, nisoldipine, ranolazine, tolvaptan, eplerenone, lovastatin, simvastatin and colchicine.

NIH; DailyMed. Current Medication Information for Nizoral (Ketoconazole) Tablet (Revised: March 2014). Available from, as of November 11, 2014: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=090660c1-6e6d-457f-adb5-046ddfcd1465


The use of Nizoral Tablets is contraindicated in patients with acute or chronic liver disease.

NIH; DailyMed. Current Medication Information for Nizoral (Ketoconazole) Tablet (Revised: March 2014). Available from, as of November 11, 2014: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=090660c1-6e6d-457f-adb5-046ddfcd1465


For more Drug Warnings (Complete) data for KETOCONAZOLE (46 total), please visit the HSDB record page.


4.4 Drug Indication

Ketoconazole HRA is indicated for the treatment of endogenous Cushings syndrome in adults and adolescents above the age of 12 years.


5 Pharmacology and Biochemistry
5.1 MeSH Pharmacological Classification

Cytochrome P-450 CYP3A Inhibitors

Drugs and compounds which inhibit or antagonize the biosynthesis or actions of CYTOCHROME P-450 CYP3A. (See all compounds classified as Cytochrome P-450 CYP3A Inhibitors.)


14-alpha Demethylase Inhibitors

Compounds that specifically inhibit STEROL 14-DEMETHYLASE. A variety of azole-derived ANTIFUNGAL AGENTS act through this mechanism. (See all compounds classified as 14-alpha Demethylase Inhibitors.)


Antifungal Agents

Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues. (See all compounds classified as Antifungal Agents.)


5.2 FDA Pharmacological Classification
5.2.1 Pharmacological Classes
Azoles [CS]; Cytochrome P450 3A4 Inhibitors [MoA]; Cytochrome P450 3A5 Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]; Azole Antifungal [EPC]
5.3 ATC Code

J02AB02


D01AC08

S76 | LUXPHARMA | Pharmaceuticals Marketed in Luxembourg | Pharmaceuticals marketed in Luxembourg, as published by d'Gesondheetskeess (CNS, la caisse nationale de sante, www.cns.lu), mapped by name to structures using CompTox by R. Singh et al. (in prep.). List downloaded from https://cns.public.lu/en/legislations/textes-coordonnes/liste-med-comm.html. Dataset DOI:10.5281/zenodo.4587355


D - Dermatologicals

D01 - Antifungals for dermatological use

D01A - Antifungals for topical use

D01AC - Imidazole and triazole derivatives

D01AC08 - Ketoconazole


G - Genito urinary system and sex hormones

G01 - Gynecological antiinfectives and antiseptics

G01A - Antiinfectives and antiseptics, excl. combinations with corticosteroids

G01AF - Imidazole derivatives

G01AF11 - Ketoconazole


H - Systemic hormonal preparations, excl. sex hormones and insulins

H02 - Corticosteroids for systemic use

H02C - Antiadrenal preparations

H02CA - Anticorticosteroids

H02CA03 - Ketoconazole


J - Antiinfectives for systemic use

J02 - Antimycotics for systemic use

J02A - Antimycotics for systemic use

J02AB - Imidazole derivatives

J02AB02 - Ketoconazole


5.4 Absorption, Distribution and Excretion

Ketoconazole is rapidly absorbed from the GI tract. Following oral administration, ketoconazole is dissolved in gastric secretions and converted to the hydrochloride salt prior to absorption from the stomach.

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014


The effect of food on the rate and extent of GI absorption of ketoconazole has not been clearly determined. Some clinicians have reported that administration of ketoconazole to fasting individuals results in higher plasma concentrations of the drug than does administration with food. However, the manufacturer states that administration of ketoconazole with food increases the extent of absorption and results in more consistent plasma concentrations of the drug. The manufacturer suggests that food increases absorption of ketoconazole by increasing the rate and/or extent of dissolution of ketoconazole (e.g., by increasing bile secretions) or by delaying stomach emptying.

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014


Ketoconazole is a weak dibasic agent and thus requires acidity for dissolution and absorption.

NIH; DailyMed. Current Medication Information for Nizoral (Ketoconazole) Tablet (Revised: March 2014). Available from, as of November 11, 2014: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=090660c1-6e6d-457f-adb5-046ddfcd1465


The bioavailability of oral ketoconazole depends on the pH of the gastric contents in the stomach; an increase in the pH results in decreased absorption of the drug. Decreased bioavailability of ketoconazole has been reported in patients with acquired immunodeficiency syndrome (AIDS), probably because of gastric hypochlorhydria associated with this condition; concomitant administration of dilute hydrochloric acid solution normalized absorption of the drug in these patients.198 Concomitant administration of an acidic beverage may increase bioavailability of oral ketoconazole in some individuals with achlorhydria.

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014


For more Absorption, Distribution and Excretion (Complete) data for KETOCONAZOLE (19 total), please visit the HSDB record page.


5.5 Metabolism/Metabolites

Ketoconazole is partially metabolized, in the liver, to several inactive metabolites by oxidation and degradation of the imidazole and piperazine rings, by oxidative O-dealkylation, and by aromatic hydroxylation.

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014


5.6 Biological Half-Life

Plasma concentrations of ketoconazole appear to decline in a biphasic manner with a half-life of approximately 2 hours in the initial phase and approximately 8 hours in the terminal phase.

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014


Elimination from plasma is biphasic with a half-life of 2 hours during the first 10 hours and 8 hours thereafter.

NIH; DailyMed. Current Medication Information for Nizoral (Ketoconazole) Tablet (Revised: March 2014). Available from, as of November 11, 2014: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=090660c1-6e6d-457f-adb5-046ddfcd1465


5.7 Mechanism of Action

Ketoconazole blocks the synthesis of ergosterol, a key component of the fungal cell membrane, through the inhibition of cytochrome P-450 dependent enzyme lanosterol 14alpha-demethylase responsible for the conversion of lanosterol to ergosterol in the fungal cell membrane. This results in an accumulation of methylated sterol precursors and a depletion of ergosterol within the cell membrane thus weakening the structure and function of the fungal cell membrane.

NIH; DailyMed. Current Medication Information for Nizoral (Ketoconazole) Tablet (Revised: March 2014). Available from, as of November 11, 2014: https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=090660c1-6e6d-457f-adb5-046ddfcd1465


Like other azole antifungal agents, ketoconazole presumably exerts its antifungal activity by altering cellular membranes, resulting in increased membrane permeability, secondary metabolic effects, and growth inhibition. Although the exact mechanism of action of ketoconazole has not been fully determined, it has been suggested that the fungistatic activity of the drug may result from interference with ergosterol synthesis, probably via inhibition of C-14 demethylation of sterol intermediates (e.g., lanosterol). The fungicidal activity of ketoconazole at high concentrations may result from a direct physiochemical effect of the drug on the fungal cell membrane.

American Society of Health-System Pharmacists 2014; Drug Information 2014. Bethesda, MD. 2014


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03-Jan-2022
30-May-2025
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DRUG PRODUCT COMPOSITIONS

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DOSAGE - TABLET;ORAL - 200MG **Federal Regist...DOSAGE - TABLET;ORAL - 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 18533

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DOSAGE - SHAMPOO;TOPICAL - 2% **Federal Regis...DOSAGE - SHAMPOO;TOPICAL - 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 19927

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DOSAGE - SHAMPOO;TOPICAL - 1%

USFDA APPLICATION NUMBER - 20310

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DOSAGE - AEROSOL, FOAM;TOPICAL - 2% **Federal...DOSAGE - AEROSOL, FOAM;TOPICAL - 2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 21738

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DOSAGE - GEL;TOPICAL - 2%

USFDA APPLICATION NUMBER - 21946

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ABOUT THIS PAGE

Looking for 65277-42-1 / Ketoconazole API manufacturers, exporters & distributors?

Ketoconazole manufacturers, exporters & distributors 1

19

PharmaCompass offers a list of Ketoconazole 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 Ketoconazole manufacturer or Ketoconazole supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ketoconazole manufacturer or Ketoconazole supplier.

PharmaCompass also assists you with knowing the Ketoconazole API Price utilized in the formulation of products. Ketoconazole API Price is not always fixed or binding as the Ketoconazole Price is obtained through a variety of data sources. The Ketoconazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Ketoconazole

Synonyms

(+)-ketoconazole, 65277-42-1, (2r,4s)-ketoconazole, 142128-59-4, Kuric, Ketocanazole

Cas Number

65277-42-1

About Ketoconazole

Broad spectrum antifungal agent used for long periods at high doses, especially in immunosuppressed patients.

NCGC00025000-05 Manufacturers

A NCGC00025000-05 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00025000-05, including repackagers and relabelers. The FDA regulates NCGC00025000-05 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00025000-05 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 NCGC00025000-05 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

NCGC00025000-05 Suppliers

A NCGC00025000-05 supplier is an individual or a company that provides NCGC00025000-05 active pharmaceutical ingredient (API) or NCGC00025000-05 finished formulations upon request. The NCGC00025000-05 suppliers may include NCGC00025000-05 API manufacturers, exporters, distributors and traders.

click here to find a list of NCGC00025000-05 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

NCGC00025000-05 USDMF

A NCGC00025000-05 DMF (Drug Master File) is a document detailing the whole manufacturing process of NCGC00025000-05 active pharmaceutical ingredient (API) in detail. Different forms of NCGC00025000-05 DMFs exist exist since differing nations have different regulations, such as NCGC00025000-05 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A NCGC00025000-05 DMF submitted to regulatory agencies in the US is known as a USDMF. NCGC00025000-05 USDMF includes data on NCGC00025000-05's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NCGC00025000-05 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of NCGC00025000-05 suppliers with USDMF on PharmaCompass.

NCGC00025000-05 JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The NCGC00025000-05 Drug Master File in Japan (NCGC00025000-05 JDMF) empowers NCGC00025000-05 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the NCGC00025000-05 JDMF during the approval evaluation for pharmaceutical products. At the time of NCGC00025000-05 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of NCGC00025000-05 suppliers with JDMF on PharmaCompass.

NCGC00025000-05 KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a NCGC00025000-05 Drug Master File in Korea (NCGC00025000-05 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of NCGC00025000-05. The MFDS reviews the NCGC00025000-05 KDMF as part of the drug registration process and uses the information provided in the NCGC00025000-05 KDMF to evaluate the safety and efficacy of the drug.

After submitting a NCGC00025000-05 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 NCGC00025000-05 API can apply through the Korea Drug Master File (KDMF).

click here to find a list of NCGC00025000-05 suppliers with KDMF on PharmaCompass.

NCGC00025000-05 CEP

A NCGC00025000-05 CEP of the European Pharmacopoeia monograph is often referred to as a NCGC00025000-05 Certificate of Suitability (COS). The purpose of a NCGC00025000-05 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of NCGC00025000-05 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of NCGC00025000-05 to their clients by showing that a NCGC00025000-05 CEP has been issued for it. The manufacturer submits a NCGC00025000-05 CEP (COS) as part of the market authorization procedure, and it takes on the role of a NCGC00025000-05 CEP holder for the record. Additionally, the data presented in the NCGC00025000-05 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the NCGC00025000-05 DMF.

A NCGC00025000-05 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. NCGC00025000-05 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 NCGC00025000-05 suppliers with CEP (COS) on PharmaCompass.

NCGC00025000-05 WC

A NCGC00025000-05 written confirmation (NCGC00025000-05 WC) is an official document issued by a regulatory agency to a NCGC00025000-05 manufacturer, verifying that the manufacturing facility of a NCGC00025000-05 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting NCGC00025000-05 APIs or NCGC00025000-05 finished pharmaceutical products to another nation, regulatory agencies frequently require a NCGC00025000-05 WC (written confirmation) as part of the regulatory process.

click here to find a list of NCGC00025000-05 suppliers with Written Confirmation (WC) on PharmaCompass.

NCGC00025000-05 NDC

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 NCGC00025000-05 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for NCGC00025000-05 API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 NCGC00025000-05 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain NCGC00025000-05 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a NCGC00025000-05 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of NCGC00025000-05 suppliers with NDC on PharmaCompass.

NCGC00025000-05 GMP

NCGC00025000-05 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 NCGC00025000-05 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 NCGC00025000-05 GMP manufacturer or NCGC00025000-05 GMP API supplier for your needs.

NCGC00025000-05 CoA

A NCGC00025000-05 CoA (Certificate of Analysis) is a formal document that attests to NCGC00025000-05's compliance with NCGC00025000-05 specifications and serves as a tool for batch-level quality control.

NCGC00025000-05 CoA mostly includes findings from lab analyses of a specific batch. For each NCGC00025000-05 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.

NCGC00025000-05 may be tested according to a variety of international standards, such as European Pharmacopoeia (NCGC00025000-05 EP), NCGC00025000-05 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NCGC00025000-05 USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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