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Chemistry

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Also known as: 98319-26-7, Proscar, Propecia, Finastid, Prostide, Chibro-proscar
Molecular Formula
C23H36N2O2
Molecular Weight
372.5  g/mol
InChI Key
DBEPLOCGEIEOCV-WSBQPABSSA-N
FDA UNII
57GNO57U7G

Finasteride
An orally active 3-OXO-5-ALPHA-STEROID 4-DEHYDROGENASE inhibitor. It is used as a surgical alternative for treatment of benign PROSTATIC HYPERPLASIA.
Finasteride is a 5-alpha Reductase Inhibitor. The mechanism of action of finasteride is as a 5-alpha Reductase Inhibitor.
1 2D Structure

Finasteride

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
(1S,3aS,3bS,5aR,9aR,9bS,11aS)-N-tert-butyl-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide
2.1.2 InChI
InChI=1S/C23H36N2O2/c1-21(2,3)25-20(27)17-8-7-15-14-6-9-18-23(5,13-11-19(26)24-18)16(14)10-12-22(15,17)4/h11,13-18H,6-10,12H2,1-5H3,(H,24,26)(H,25,27)/t14-,15-,16-,17+,18+,22-,23+/m0/s1
2.1.3 InChI Key
DBEPLOCGEIEOCV-WSBQPABSSA-N
2.1.4 Canonical SMILES
CC12CCC3C(C1CCC2C(=O)NC(C)(C)C)CCC4C3(C=CC(=O)N4)C
2.1.5 Isomeric SMILES
C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2C(=O)NC(C)(C)C)CC[C@@H]4[C@@]3(C=CC(=O)N4)C
2.2 Other Identifiers
2.2.1 UNII
57GNO57U7G
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Chibro Proscar

2. Chibro-proscar

3. Eucoprost

4. Mk 906

5. Mk-906

6. Mk906

7. Propecia

8. Propeshia

9. Proscar

2.3.2 Depositor-Supplied Synonyms

1. 98319-26-7

2. Proscar

3. Propecia

4. Finastid

5. Prostide

6. Chibro-proscar

7. Mk-906

8. Finpecia

9. Finasterida

10. Finasteridum

11. Mk 906

12. (5alpha,17beta)-(1,1-dimethylethyl)-3-oxo-4-azaandrost-1-ene-17-carboxamide

13. (4ar,4bs,6as,7s,9as,9bs,11ar)-n-tert-butyl-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxamide

14. Chembl710

15. Nsc-741485

16. N-tert-butyl-3-oxo-4-aza-5alpha-androst-1-ene-17beta-carboxamide

17. 57gno57u7g

18. Chebi:5062

19. (1s,3as,3bs,5ar,9ar,9bs,11as)-n-tert-butyl-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide

20. (4ar,4bs,6as,7s,9as,9bs,11ar)-n-(tert-butyl)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxamide

21. Nsc-759318

22. Finasteridum [inn-latin]

23. Finasterida [inn-spanish]

24. Dsstox_cid_625

25. Dsstox_rid_75699

26. Dsstox_gsid_20625

27. (4ar,4bs,6as,7s,9as,9bs,11ar)-n-(1,1-dimethylethyl)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxamide

28. N-tert-butyl-3-oxo-4-aza-5alpha-androst-1-en-17beta-carboxamide

29. Andozac

30. 4-azaandrost-1-ene-17-carboxamide, N-(1,1-dimethylethyl)-3-oxo-, (5alpha,17beta)-

31. Propecia (tn)

32. Smr000466304

33. Proscar (tn)

34. Mk 0906

35. Mk-0906

36. Ccris 7438

37. Hsdb 6793

38. Mk906

39. Sr-01000759414

40. Brn 4269024

41. Unii-57gno57u7g

42. L-652,931

43. 17beta-(n-tert-butylcarbamoyl)-4-aza-5 Alpha-androst-1-en-3-one

44. Ncgc00016965-01

45. Finasteride [usan:usp:inn:ban]

46. N-(2-methyl-2-propyl)-3-oxo-4-aza-5-alpha-androst-1-ene-17-beta-carboxamide

47. Cas-98319-26-7

48. Mfcd00869737

49. Ym-152

50. Ks-1058

51. Finasteride (proscar)

52. Finasteride [mi]

53. Prestwick0_000717

54. Prestwick1_000717

55. Prestwick2_000717

56. Prestwick3_000717

57. Finasteride [inn]

58. Finasteride [jan]

59. Finasteride [usan]

60. Finasteride [vandf]

61. Schembl5509

62. Finasteride [mart.]

63. Bspbio_000933

64. Finasteride [who-dd]

65. Mls000759404

66. Mls001165768

67. Mls001424046

68. Finasteride (jan/usp/inn)

69. Spbio_002854

70. Bpbio1_001027

71. Gtpl6818

72. Dtxsid3020625

73. N-tert-butyl-3-oxo-4-aza-5.alpha.-androst-1-ene-17.beta.-carboxamide

74. Finasteride [ep Impurity]

75. Finasteride [orange Book]

76. 4-azaandrost-1-ene-17-carboxamide, N-(1,1-dimethylethyl)-3-oxo-, (5.alpha.,17.beta.)-

77. Bcpp000229

78. Finasteride [ep Monograph]

79. Finasteride [usp Impurity]

80. Hms1570o15

81. Hms2051f09

82. Hms2090g22

83. Hms2097o15

84. Hms2235l23

85. Hms3714o15

86. Finasteride [usp Monograph]

87. 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide

88. Act02599

89. Entadfi Component Finasteride

90. Ex-a1951

91. Zinc3782599

92. Tox21_110717

93. Tox21_201506

94. Tox21_302744

95. Bdbm50334788

96. Nsc741485

97. Nsc757443

98. S1197

99. Akos015894916

100. Tox21_110717_1

101. Bcp9000685

102. Ccg-100937

103. Cs-1767

104. Db01216

105. Finasteride Component Of Entadfi

106. Finasteride, >=98% (hplc), Powder

107. Nc00187

108. Nsc 741485

109. Nsc 759318

110. Nsc-757443

111. Ncgc00093560-05

112. Ncgc00256334-01

113. Ncgc00259057-01

114. 140375-21-9

115. Bf164456

116. Cpd000466304

117. Hy-13635

118. Bcp0726000222

119. Ab00513901

120. D00321

121. Ab00513901-07

122. Ab00513901-08

123. Ab00513901_09

124. Finasteride, Vetranal(tm), Analytical Standard

125. 319f267

126. A845840

127. Q424167

128. Sr-01000759414-4

129. Sr-01000759414-6

130. Brd-k01095011-001-03-5

131. Brd-k01095011-001-15-9

132. Finasteride, British Pharmacopoeia (bp) Reference Standard

133. Finasteride, European Pharmacopoeia (ep) Reference Standard

134. ([1-phenyl-meth-(e)-ylidene]-amino)-aceticacidethylester

135. (17beta-(n-tert-butylcarbamoyl)-4-aza-5alpha-androst-1-en-3-one

136. Finasteride, United States Pharmacopeia (usp) Reference Standard

137. (5?,17?)-n-(1,1-dimethylethyl)-3-oxo-4-azaandrost-1-ene-17-carboxamide

138. 4-azaandrost-1-ene-17-carboxamide,1-dimethylethyl)-3-oxo-, (5.alpha., 17.beta.)-

139. Finasteride For Peak Identification, European Pharmacopoeia (ep) Reference Standard

140. (1s,2r,7r,10s,11s,14s,15s)-n-tert-butyl-2,15-dimethyl-5-oxo-6-azatetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-3-ene-14-carboxamide

141. (1s,3as,3bs,5ar,9ar,9bs,11as)-n-isobutyl-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide

142. (1s,3as,3bs,5ar,9ar,9bs,11as)-n-isobutyl-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide;finasteride

143. (4ar,4bs,6as,7s,9as,9bs,11ar)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide

144. (4ar,4bs,6as,9as,9bs,11ar)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide

145. (4ar,6as)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide

146. (4ar,6as,11ar)-4a,6a-dimethyl-2-oxo-hexadecahydro-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide

147. (4ar,6as,7s)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide

148. (4ar,6as,7s,11ar)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide

149. (r)-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide

150. 1h-indeno[5,4-f]quinoline-7-carboxamide, N-(1,1-dimethylethyl)-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-4a,6a-dimethyl-2-oxo-, (4ar,4bs,6as,7s,9as,9bs,11ar)-

151. 4a,6a,9a-trimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid (finasteride)

152. 4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1h-indeno[5,4-f]quinoline-7-carboxylic Acid Tert-butylamide(finasteride)

2.4 Create Date
2005-06-24
3 Chemical and Physical Properties
Molecular Weight 372.5 g/mol
Molecular Formula C23H36N2O2
XLogP33
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass372.277678395 g/mol
Monoisotopic Mass372.277678395 g/mol
Topological Polar Surface Area58.2 Ų
Heavy Atom Count27
Formal Charge0
Complexity678
Isotope Atom Count0
Defined Atom Stereocenter Count7
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 6  
Drug NameFinasteride
PubMed HealthFinasteride (By mouth)
Drug ClassesAlopecia Agent, Benign Prostatic Hypertrophy Agent
Drug LabelFinasteride, USP, a synthetic 4-azasteroid compound, is a specific inhibitor of steroid Type II 5-reductase, an intracellular enzyme that converts the androgen testosterone into 5-dihydrotestosterone (DHT).Finasteride is 4-Azaandrost-1-ene-17-car...
Active IngredientFinasteride
Dosage FormTablet
Routeoral; Oral
Strength5mg; 1mg
Market StatusTentative Approval; Prescription
CompanyWatson Labs; Mylan Pharms; Actavis Elizabeth; Teva; Accord Hlthcare; Hetero Labs Ltd Iii; Aurobindo Pharma; Zydus Pharms Usa; Dr Reddys Labs; Gedeon Richter Usa; Sun Pharma Global; Mylan

2 of 6  
Drug NamePropecia
PubMed HealthFinasteride (By mouth)
Drug ClassesAlopecia Agent, Benign Prostatic Hypertrophy Agent
Drug LabelPROPECIA (finasteride) tablets contain finasteride as the active ingredient. Finasteride, a synthetic 4-azasteroid compound, is a specific inhibitor of steroid Type II 5-reductase, an intracellular enzyme that converts the androgen testosterone int...
Active IngredientFinasteride
Dosage FormTablet
RouteOral
Strength1mg
Market StatusPrescription
CompanyMerck

3 of 6  
Drug NameProscar
Drug LabelPROSCAR (finasteride), a synthetic 4-azasteroid compound, is a specific inhibitor of steroid Type II 5-reductase, an intracellular enzyme that converts the androgen testosterone into 5-dihydrotestosterone (DHT).Finasteride is 4-azaandrost-1-ene-1...
Active IngredientFinasteride
Dosage FormTablet
RouteOral
Strength5mg
Market StatusPrescription
CompanyMerck

4 of 6  
Drug NameFinasteride
PubMed HealthFinasteride (By mouth)
Drug ClassesAlopecia Agent, Benign Prostatic Hypertrophy Agent
Drug LabelFinasteride, USP, a synthetic 4-azasteroid compound, is a specific inhibitor of steroid Type II 5-reductase, an intracellular enzyme that converts the androgen testosterone into 5-dihydrotestosterone (DHT).Finasteride is 4-Azaandrost-1-ene-17-car...
Active IngredientFinasteride
Dosage FormTablet
Routeoral; Oral
Strength5mg; 1mg
Market StatusTentative Approval; Prescription
CompanyWatson Labs; Mylan Pharms; Actavis Elizabeth; Teva; Accord Hlthcare; Hetero Labs Ltd Iii; Aurobindo Pharma; Zydus Pharms Usa; Dr Reddys Labs; Gedeon Richter Usa; Sun Pharma Global; Mylan

5 of 6  
Drug NamePropecia
PubMed HealthFinasteride (By mouth)
Drug ClassesAlopecia Agent, Benign Prostatic Hypertrophy Agent
Drug LabelPROPECIA (finasteride) tablets contain finasteride as the active ingredient. Finasteride, a synthetic 4-azasteroid compound, is a specific inhibitor of steroid Type II 5-reductase, an intracellular enzyme that converts the androgen testosterone int...
Active IngredientFinasteride
Dosage FormTablet
RouteOral
Strength1mg
Market StatusPrescription
CompanyMerck

6 of 6  
Drug NameProscar
Drug LabelPROSCAR (finasteride), a synthetic 4-azasteroid compound, is a specific inhibitor of steroid Type II 5-reductase, an intracellular enzyme that converts the androgen testosterone into 5-dihydrotestosterone (DHT).Finasteride is 4-azaandrost-1-ene-1...
Active IngredientFinasteride
Dosage FormTablet
RouteOral
Strength5mg
Market StatusPrescription
CompanyMerck

4.2 Therapeutic Uses

Enzyme Inhibitors

National Library of Medicine's Medical Subject Headings online file (MeSH, 1999)


Treatment of benign prostatic hypertrophy

Budavari, S. (ed.). The Merck Index - Encyclopedia of Chemicals, Drugs and Biologicals. Rahway, NJ: Merck and Co., Inc., 1989., p. 1250


Antiandrogen therapy appears to produce a 30 to 40% decrease in the volume of the hyperplastic prostate after 3 to 6 months of therapy. Longer treatment may result in further prostatic regression, although this remains to be seen. Biopsy studies suggest that epithelial regression occurs to a much more significant degree than does stromal regression, but this finding may simply reflect the relatively longer turnover of the stromal cell population. The significant placebo effect of oral medication in patients with benign prostatic hyperplasia makes interpretation of clinical symptomatology and uro-flow data difficult. Analysis of symptom improvement is further complicated by the relatively slow improvement of patients on antiandrogen therapy, in contrast to surgery, in which relief is immediate. In addition to limited stromal involution and inadequate treatment duration, other biologic factors may limit the clinical efficacy of antiandrogen therapy. Most importantly, prostatic involution may not necessarily decrease urethral resistance. In addition, obstruction induced detrusor dysfunction may persist after relief of outflow obstruction in some patients, as it does after surgery. Incomplete antiandrogen action of the compounds, as well as compliance issues, may likewise limit efficacy. Although there are no data to suggest that the 5 alpha-reductase inhibitor finasteride will be more effective than other antiandrogen compounds in the treatment of benign prostatic hyperplasia, preliminary studies suggest that it has less toxicity. If long-term studies validate a modest but significant clinical response rate and preservation of sexual function, then finasteride therapy may well be acceptable to a subgroup of men presenting with the symptoms of benign prostatic hyperplasia.

PMID:1695786 McConnell JD; Urol Clin North Am 17 (3): 661-70 (1990)


4.3 Drug Indication

Finasteride is indicated for the treatment of symptomatic benign prostatic hyperplasia (BPH) in men with an enlarged prostate to improve symptoms, reduce the risk of acute urinary retention, and reduce the risk of the need for surgery including transurethral resection of the prostate (TURP) and prostatectomy. A combination product with [tadalafil] is also used for the symptomatic treatment of BPH for up to 26 weeks. Finasteride is also indicated for the treatment of male pattern hair loss (androgenetic alopecia, hereditary alopecia, or common male baldness) in male patients.


Treatment of androgenetic alopecia


5 Pharmacology and Biochemistry
5.1 Pharmacology

Finasteride is an antiandrogenic compound that works by suppressing the production of serum and intraprostatic dihydrotestosterone (DHT) in men via inhibiting the enzyme responsible for the biosynthesis of DHT. The maximum effect of a rapid reduction in serum DHT concentration is expected to be observed 8 hours following administration of the first dose. In a single man receiving a single oral dose of 5 mg finasteride for up to 4 years, there was a reduction in the serum DHT concentrations by approximately 70% and the median circulating level of testosterone increased by approximately 10-20% within the physiologic range. In a double-blind, placebo-controlled study, finasteride reduced intraprostatic DHT level by 91.4% but finasteride is not expected to decrease the DHT levels to castrate levels since circulating testosterone is also converted to DHT by the type 1 isoenzyme expressed in other tissues. It is expected that DHT levels return to normal within 14 days upon discontinuation of the drug. In a study of male patients with benign prostatic hyperplasia prior to prostatectomy, the treatment with finasteride resulted in an approximate 80% lower DHT content was measured in prostatic tissue removed at surgery compared to placebo. While finasteride reduces the size of the prostate gland by 20%, this may not correlate well with improvement in symptoms. The effects of finasteride are reported to be more pronounced in male patients with enlarged prostates (>25 mL) who are at the greatest risk of disease progression. In phase III clinical studies, oral administration of finasteride in male patients with male pattern hair loss promoted hair growth and prevented further hair loss by 66% and 83% of the subjects, respectively, which lasted during two years' treatment. The incidences of these effects in treatment groups were significantly higher than that of the group receiving a placebo. Following finasteride administration, the levels of DHT in the scalp skin was shown to be reduced by more than 60%, indicating that the DHT found in scalp is derived from both local DHT production and circulating DHT. The effect of finasteride on scalp DHT is likely seen because of its effect on both local follicular DHT levels as well as serum DHT levels.. There is evidence from early clinical observations and controlled studies that finasteride may reduce bleeding of prostatic origin.


5.2 MeSH Pharmacological Classification

Urological Agents

Drugs used in the treatment of urological conditions and diseases such as URINARY INCONTINENCE and URINARY TRACT INFECTIONS. (See all compounds classified as Urological Agents.)


5-alpha Reductase Inhibitors

Drugs that inhibit 3-OXO-5-ALPHA-STEROID 4-DEHYDROGENASE. They are commonly used to reduce the production of DIHYDROTESTOSTERONE. (See all compounds classified as 5-alpha Reductase Inhibitors.)


5.3 FDA Pharmacological Classification
5.3.1 Active Moiety
FINASTERIDE
5.3.2 FDA UNII
57GNO57U7G
5.3.3 Pharmacological Classes
5-alpha Reductase Inhibitors [MoA]; 5-alpha Reductase Inhibitor [EPC]
5.4 ATC Code

G04CB01

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

D11 - Other dermatological preparations

D11A - Other dermatological preparations

D11AX - Other dermatologicals

D11AX10 - Finasteride


G - Genito urinary system and sex hormones

G04 - Urologicals

G04C - Drugs used in benign prostatic hypertrophy

G04CB - Testosterone-5-alpha reductase inhibitors

G04CB01 - Finasteride


5.5 Absorption, Distribution and Excretion

Absorption

Finasteride is well absorbed following oral administration and displays a slow accumulation phase after multiple dosing.[lablel] In healthy male subjects receiving oral finasteride, the mean oral bioavailability was 65% for 1 mg finasteride and 63% for 5 mg finasteride, and the values ranged from 26 to 170% for 1 mg dose and from 34 to 108% for 5 mg dose, respectively. It is reported that food intake does not affect the oral bioavailability of the drug. The peak plasma concentrations (Cmax) averaged 37 ng/mL (range, 27-49 ng/mL) and was reached 1-2 hours post administration. The AUC(0-24 hr) was 53 ngxhr/mL (range, 20-154 ngxhr/mL). The plasma concentrations and AUC are reported to be higher in elderly male patients aged 70 years or older.


Route of Elimination

In healthy subjects, about 32-46% of total oral dose of finasteride was excreted in the urine in the form of metabolites while about 51-64% of the dose was excreted in the feces. In patients with renal impairment, the extent of urinary excretion of finasteride is expected to be decreased while the fecal excretion is increased.


Volume of Distribution

The volume of distribution is 76 L at steady state, ranging from 44 to 96 L. Finasteride has been shown to cross the blood brain barrier but does not appear to distribute preferentially to the CSF. It is not known whether finasteride is excreted in human milk.


Clearance

In healthy young subjects (n=15), the mean plasma clearance of finasteride was 165 mL/min with the range between 70 and 279 mL/min.


5.6 Metabolism/Metabolites

Finasteride undergoes extensive hepatic metabolism predominantly mediated by the cytochrome P450 3A4 (CYP3A4) enzyme to form the t-butyl side chain monohydroxylated and monocarboxylic acid metabolites. Theses metabolites retain less than 20% of the pharmacological activity of the parent compound.


Finasteride has known human metabolites that include N-(1-Hydroxy-2-methylpropan-2-yl)-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide.

S73 | METXBIODB | Metabolite Reaction Database from BioTransformer | DOI:10.5281/zenodo.4056560


5.7 Biological Half-Life

In healthy young subjects receiving finasteride, the mean elimination half-life in plasma was 6 hours ranging from 3 to 16 hours. In elderly patients over the age of 70 years, the half-life is prolonged to 8 hours.


5.8 Mechanism of Action

Finasteride acts as a competitive and specific inhibitor of Type II 5-reductase, a nuclear-bound steroid intracellular enzyme primarily located in the prostatic stromal cell that converts the androgen testosterone into the more active metabolite, 5-dihydrotestosterone (DHT). DHT is considered to be the primary androgen playing a role in the development and enlargement of the prostate gland. It serves as the hormonal mediator for the hyperplasia upon accumulation within the prostate gland. DHT displays a higher affinity towards androgen receptors in the prostate gland compared to testosterone and by acting on the androgen receptors, DHT modulates genes that are responsible for cell proliferation. Responsible for the production of DHT together with type I 5-reductase, the type II 5-reductase isozyme is primarily found in the prostate, seminal vesicles, epididymides, and hair follicles as well as liver. Although finasteride is 100-fold more selective for type II 5-reductase than for the type I isoenzyme, chronic treatment with this drug may have some effect on type I 5-reductase, which is predominantly expressed in sebaceous glands of most regions of skin, including the scalp, and liver. It is proposed that the type I 5-reductase and type II 5-reductase is responsible for the production of one-third and two-thirds of circulating DHT, respectively. The mechanism of action of Finasteride is based on its preferential inhibition of Type II 5-reductase through the formation of a stable complex with the enzyme _in vitro_ and _in vivo_. Finasteride works selectively, where it preferentially displays a 100-fold selectivity for the human Type II 5-reductase over type I enzyme. Inhibition of Type II 5-reductase blocks the peripheral conversion of testosterone to DHT, resulting in significant decreases in serum and tissue DHT concentrations, minimal to moderate increase in serum testosterone concentrations, and substantial increases in prostatic testosterone concentrations. As DHT appears to be the principal androgen responsible for stimulation of prostatic growth, a decrease in DHT concentrations will result in a decrease in prostatic volume (approximately 20-30% after 6-24 months of continued therapy). It is suggested that increased levels of DHT can lead to potentiated transcription of prostaglandin D2, which promotes the proliferation of prostate cancer cells. In men with androgenic alopecia, the mechanism of action has not been fully determined, but finasteride has shown to decrease scalp DHT concentration to the levels found in the hairy scalp, reduce serum DHT, increase hair regrowth, and slow hair loss. Another study suggests that finasteride may work to reduce bleeding of prostatic origin by inhibiting vascular endothelial growth factor (VEGF) in the prostate, leading to atrophy and programmed cell death. This may bestow the drug therapeutic benefits in patients idiopathic prostatic bleeding, bleeding during anticoagulation, or bleeding after instrumentation.


API SUPPLIERS

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01

Octavius Pharma Pvt. Ltd

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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02

LGM Pharma

U.S.A

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Virtual BoothLGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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03

Dr. Reddy's Laboratories

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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04

Jai Radhe Sales

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Virtual BoothJai Radhe Sales is your partner for all your sourcing needs.

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Jai Radhe Sales

05

HRV Global Life Sciences

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Virtual BoothHRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.

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HRV Global Life Sciences

06

Dr. Reddy's Laboratories

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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07

Hubei Gedian Humanwell Pharmaceuti...

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Pharmex
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Hubei Gedian Humanwell Pharmaceuti...

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Hubei Gedian Humanwell Pharmaceuti...

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Pharmex
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Hubei Gedian Humanwell Pharmaceuti...

China

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Sun Pharmaceutical Industries Limi...

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Pharmex
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Sun Pharmaceutical Industries Limi...

India

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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Gedeon Richter

Hungary

USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

Pharmex
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Gedeon Richter

Hungary

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USDMF

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GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 16010

Submission : 2002-06-11

Status : Active

Type : II

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02

Pharmex
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02

Pharmex
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GDUFA

DMF Review : Complete

Rev. Date : 2013-02-27

Pay. Date : 2013-01-22

DMF Number : 19308

Submission : 2006-03-27

Status : Active

Type : II

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Cipla Ltd

India

USDMF

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Cipla Ltd

India
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GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 15778

Submission : 2001-12-28

Status : Active

Type : II

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Cipla Ltd

India

USDMF

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04

Cipla Ltd

India
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GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 17680

Submission : 2004-09-09

Status : Inactive

Type : II

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Gedeon Richter Plc

Hungary

USDMF

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Pharmex
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GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 17575

Submission : 2004-07-26

Status : Inactive

Type : II

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Hetero Labs Ltd

India

USDMF

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GDUFA

DMF Review : Complete

Rev. Date : 2014-05-16

Pay. Date : 2014-05-05

DMF Number : 20893

Submission : 2007-09-27

Status : Active

Type : II

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Pharmex
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GDUFA

DMF Review : Complete

Rev. Date : 2013-04-24

Pay. Date : 2012-12-05

DMF Number : 21276

Submission : 2008-01-21

Status : Active

Type : II

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Sterling Spa

Italy

USDMF

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Sterling Spa

Italy
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GDUFA

DMF Review : N/A

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Submission : 2005-07-06

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KDMF

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Finasteride

Registrant Name : Sangjin Corporation

Registration Date : 2008-11-28

Registration Number : 20081128-94-E-29-06

Manufacturer Name : Dr. Reddy's Laboratories Ltd...

Manufacturer Address : Plot No. 110 & 111, SVCo.operative Industrial Estate, Bollaram Village, _x000D_ Jinna...

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02

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Finasteride

Registrant Name : Samoh Pharmaceutical Co., Ltd.

Registration Date : 2021-08-17

Registration Number : 20071025-94-E-50-02(11)

Manufacturer Name : Aurobindo Pharma Limited

Manufacturer Address : Unit - VIII, Survey No. : 10 & 13 Gaddapotharam(Village), IDA - Kazipally, Jinnaram (...

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03

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Finasteride

Registrant Name : Grand Biopharm Co., Ltd.

Registration Date : 2025-05-20

Registration Number : 20071025-94-E-50-02(13)

Manufacturer Name : Apitoria Pharma Private Limi...

Manufacturer Address : Survey No. : 10 & 13 Gaddapotharam(Village), IDA - Kazipally, Jinnaram (Mandal), Sang...

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04

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Finasteride

Registrant Name : The One Pharmtech Co., Ltd.

Registration Date : 2023-05-30

Registration Number : 20071025-94-E-50-02(12)

Manufacturer Name : Aurobindo Pharma Limited

Manufacturer Address : Unit - VIII, Survey No. : 10 & 13 Gaddapotharam(Village), IDA - Kazipally, Jinnaram (...

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05

Cipla

India
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Cipla

India
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Finasteride

Registrant Name : Hiple Co., Ltd.

Registration Date : 2021-03-12

Registration Number : 20071228-94-E-57-03(9)

Manufacturer Name : Cipla Limited

Manufacturer Address : A-33 & A-37/2/2, MIDC Patalganga - 410 220, District Raigad, Maharashtra, State, Indi...

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06

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Finasteride

Registrant Name : Pharmapia Co., Ltd.

Registration Date : 2024-10-07

Registration Number : 20220511-94-E-173-14(1)

Manufacturer Name : MSN Laboratories Private Lim...

Manufacturer Address : Sy. No. 317, 320, 321, 322, 323, 604 & 605, Rudraram (Village), Patancheru (Mandal), ...

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07

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Finasteride

Registrant Name : Kukjeon Pharmaceutical Co., Ltd.

Registration Date : 2022-05-11

Registration Number : 20220511-94-E-173-14

Manufacturer Name : MSN Laboratories Private Lim...

Manufacturer Address : Sy. No. 317, 320, 321, 322, 323, 604 & 605, Rudraram (Village), Patancheru (Mandal), ...

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08

Sterling Spa

Italy
Pharmex
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Sterling Spa

Italy
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Finasteride

Registrant Name : Boryeong Co., Ltd.

Registration Date : 2021-10-26

Registration Number : 20211026-94-E-172-13

Manufacturer Name : Sterling SPA@IMS srl@Microch...

Manufacturer Address : Via della Carboneria 30 (loc. Solomeo) - 06073 Corciano Perugia, Italy@Via Venezia Gi...

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09

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Finasteride

Registrant Name : Sanil Pharma Co., Ltd.

Registration Date : 2025-06-23

Registration Number : 20250623-94-E-188-16

Manufacturer Name : Swati Spentose Private Limit...

Manufacturer Address : Plot No. A-1/2110-2111, III Phase, GIDC VAPI, City: Vapi - 396 195, Dist. Valsad, Guj...

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10

Pharmex
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Finasteride

Registrant Name : Aging Life Science Co., Ltd.

Registration Date : 2025-06-02

Registration Number : 20250602-94-E-191-17

Manufacturer Name : Shakti Lifescience Private L...

Manufacturer Address : Plot No. K-2, K-1 MIDC, Tarapur, Dist. Palghar Boisar Taluka Palghar 401506, Maharash...

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NDC API

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01

Pharmex
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FINASTERIDE

NDC Package Code : 65862-370

Start Marketing Date : 2023-12-15

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (50kg/50kg)

Marketing Category : BULK INGREDIENT

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02

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

FINASTERIDE

NDC Package Code : 71052-602

Start Marketing Date : 2017-06-01

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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03

Pharmex
Not Confirmed
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Pharmex
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FINASTERIDE

NDC Package Code : 68554-0022

Start Marketing Date : 1992-06-19

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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04

Pharmex
Not Confirmed
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FINASTERIDE

NDC Package Code : 62991-3175

Start Marketing Date : 2022-10-17

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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05

Medisca Inc.

U.S.A
Pharmex
Not Confirmed
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Medisca Inc.

U.S.A
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Pharmex
Not Confirmed

FINASTERIDE

NDC Package Code : 38779-2410

Start Marketing Date : 2006-08-03

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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06

Pharmex
Not Confirmed
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Pharmex
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FINASTERIDE

NDC Package Code : 51927-4847

Start Marketing Date : 2014-10-21

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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07

Pharmex
Not Confirmed
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FINASTERIDE

NDC Package Code : 82393-306

Start Marketing Date : 2023-10-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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08

Pharmex
Not Confirmed
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Pharmex
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FINASTERIDE

NDC Package Code : 73774-025

Start Marketing Date : 2025-02-14

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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09

STERLING SPA

Italy
Pharmex
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STERLING SPA

Italy
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Pharmex
Not Confirmed

FINASTERIDE

NDC Package Code : 64918-0422

Start Marketing Date : 2014-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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10

Pharmex
Not Confirmed
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FINASTERIDE

NDC Package Code : 10695-151

Start Marketing Date : 2023-06-20

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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API Reference Price

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[{"dataSource":"API Export","activeIngredients":"","year":"2022","qtr":"Q1","strtotime":1641493800,"product":"FINASTERIDE","address":"PLOT NO.2, MAITRIVIHAR BEHIND MAITRIVANAM, AMEERPET","city":"HYDERABAD","supplier":"AUROBINDO PHARMA LTD","supplierCountry":"INDIA","foreign_port":"LEIPZIG\/HALLE","customer":"HELLMANN WORLD LOGISTICS GMBH CO","customerCountry":"GERMANY","quantity":"4.00","actualQuantity":"4","unit":"KGS","unitRateFc":"4500","totalValueFC":"17585.4","currency":"USD","unitRateINR":327500,"date":"07-Jan-2022","totalValueINR":"1310000","totalValueInUsd":"17585.4","indian_port":"HYDERABAD AIR","hs_no":"29241900","bill_no":"7313014","productDescription":"API","marketType":"REGULATED MARKET","country":"GERMANY","selfForZScoreResived":"Pharma Grade","supplierPort":"HYDERABAD AIR","supplierAddress":"PLOT NO.2, MAITRIVIHAR BEHIND MAITRIVANAM, AMEERPET, HYDERABAD","customerAddress":""},{"dataSource":"API Export","activeIngredients":"","year":"2022","qtr":"Q1","strtotime":1642012200,"product":"FINASTERIDE USP","address":"HETERO CORPORATE, NO. 7-2-A2, INDUSTRIAL ESTATE,SANATHNAGAR Conta","city":"HYDERABAD","supplier":"HETERO LABS LTD","supplierCountry":"INDIA","foreign_port":"MEXICO CITY","customer":"AMAROX PHARMASA DE CV","customerCountry":"MEXICO","quantity":"63.02","actualQuantity":"63.02","unit":"KGS","unitRateFc":"2450","totalValueFC":"150644.1","currency":"USD","unitRateINR":178070.4538241828,"date":"13-Jan-2022","totalValueINR":"11222000","totalValueInUsd":"150644.1","indian_port":"HYDERABAD AIR","hs_no":"29372900","bill_no":"7444776","productDescription":"API","marketType":"","country":"MEXICO","selfForZScoreResived":"Pharma Grade","supplierPort":"HYDERABAD AIR","supplierAddress":"HETERO CORPORATE, NO. 7-2-A2, INDUSTRIAL ESTATE,SANATHNAGAR Conta, HYDERABAD","customerAddress":""},{"dataSource":"API Export","activeIngredients":"","year":"2022","qtr":"Q1","strtotime":1643653800,"product":"FINASTERIDE (TAX INV NO:1900216204 DT:29","address":"MSN HOUSE, PLOT NO. C-24,INDUSTRIAL HYDERABAD","city":"HYDERABAD","supplier":"MSN LABORATORIES PRIVATE LTD","supplierCountry":"INDIA","foreign_port":"BARCELONA","customer":"AIRPHARM BARCELONA BONDED WAREHOUSE","customerCountry":"SPAIN","quantity":"20.00","actualQuantity":"20","unit":"KGS","unitRateFc":"3217.5","totalValueFC":"62849.5","currency":"USD","unitRateINR":235550,"date":"01-Feb-2022","totalValueINR":"4711000","totalValueInUsd":"62849.5","indian_port":"HYDERABAD AIR","hs_no":"29372900","bill_no":"7908013","productDescription":"API","marketType":"REGULATED MARKET","country":"SPAIN","selfForZScoreResived":"Pharma Grade","supplierPort":"HYDERABAD AIR","supplierAddress":"MSN HOUSE, PLOT NO. 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07-Jan-2022
27-May-2025
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Drugs in Development

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Details:

Akums gains rights for patented topical formulation, Therapy-07, for the Indian market which combines three medicaments (finasteride,latanoprost,minoxidil) to combat alopecia.


Lead Product(s): Finasteride,Latanoprost,Minoxidil

Therapeutic Area: Dermatology Brand Name: Therapy-07

Study Phase: Phase IIProduct Type: Other Small Molecule

Sponsor: Akums Drugs & Pharmaceuticals Ltd

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement October 16, 2024

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01

Triple Hair

U.S.A
arrow
Pharmex
Not Confirmed

Triple Hair

U.S.A
arrow
Pharmex
Not Confirmed

Details : Akums gains rights for patented topical formulation, Therapy-07, for the Indian market which combines three medicaments (finasteride,latanoprost,minoxidil) to combat alopecia.

Product Name : Therapy-07

Product Type : Other Small Molecule

Upfront Cash : Undisclosed

October 16, 2024

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Details:

The combined company will focus on the R&D and commercialization of proprietary science and technologies for therapeutics, including Entadfi, a once-daily, oral treatment for BPH that combines finasteride, a 5α-reductase inhibitor, and tadalafil, a PDE5 inhibitor.


Lead Product(s): Finasteride,Tadalafil

Therapeutic Area: Urology Brand Name: Entadfi

Study Phase: Approved FDFProduct Type: Other Small Molecule

Sponsor: Blue Water Vaccines

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Acquisition December 18, 2023

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02

Onconetix

U.S.A
arrow
Pharmex
Not Confirmed

Onconetix

U.S.A
arrow
Pharmex
Not Confirmed

Details : The combined company will focus on the R&D and commercialization of proprietary science and technologies for therapeutics, including Entadfi, a once-daily, oral treatment for BPH that combines finasteride, a 5α-reductase inhibitor, and tadalafil, a PDE5...

Product Name : Entadfi

Product Type : Other Small Molecule

Upfront Cash : Undisclosed

December 18, 2023

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Details:

Under the collaboration, Blue Water Biotech and IQVIA will market Blue Water’s commercial portfolio including, Entadfi, an FDA-approved, once daily pill that combines finasteride and tadalafil for benign prostatic hyperplasia and Zontivity (vorapaxar).


Lead Product(s): Finasteride,Tadalafil

Therapeutic Area: Urology Brand Name: Entadfi

Study Phase: Approved FDFProduct Type: Other Small Molecule

Sponsor: IQVIA

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Collaboration June 21, 2023

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03

Pharmex
Not Confirmed
Pharmex
Not Confirmed

Details : Under the collaboration, Blue Water Biotech and IQVIA will market Blue Water’s commercial portfolio including, Entadfi, an FDA-approved, once daily pill that combines finasteride and tadalafil for benign prostatic hyperplasia and Zontivity (vorapaxar).

Product Name : Entadfi

Product Type : Other Small Molecule

Upfront Cash : Undisclosed

June 21, 2023

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Details:

The acquisition transforms the Company into a broader pharmaceutical company spanning multiple sectors by including ENTADFI (finasteride), an oral, once daily treatment for BPH that combines finasteride, a 5α-reductase inhibitor, and tadalafil, a PDE5 inhibitor.


Lead Product(s): Finasteride,Tadalafil

Therapeutic Area: Urology Brand Name: Entadfi

Study Phase: Approved FDFProduct Type: Other Small Molecule

Sponsor: Blue Water Vaccines

Deal Size: $100.0 million Upfront Cash: $20.0 million

Deal Type: Agreement April 20, 2023

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04

Veru

U.S.A
arrow
Pharmex
Not Confirmed

Veru

U.S.A
arrow
Pharmex
Not Confirmed

Details : The acquisition transforms the Company into a broader pharmaceutical company spanning multiple sectors by including ENTADFI (finasteride), an oral, once daily treatment for BPH that combines finasteride, a 5α-reductase inhibitor, and tadalafil, a PDE5 i...

Product Name : Entadfi

Product Type : Other Small Molecule

Upfront Cash : $20.0 million

April 20, 2023

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Details:

ENTADFI (finasteride and tadalafil) capsules for oral use, a new treatment for urinary tract symptoms caused by an enlarged prostate called benign prostatic hyperplasia.


Lead Product(s): Finasteride,Tadalafil

Therapeutic Area: Urology Brand Name: Entadfi

Study Phase: Approved FDFProduct Type: Other Small Molecule

Sponsor: Inapplicable

Deal Size: Inapplicable Upfront Cash: Inapplicable

Deal Type: Inapplicable December 13, 2021

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05

Veru

U.S.A
arrow
Pharmex
Not Confirmed

Veru

U.S.A
arrow
Pharmex
Not Confirmed

Details : ENTADFI (finasteride and tadalafil) capsules for oral use, a new treatment for urinary tract symptoms caused by an enlarged prostate called benign prostatic hyperplasia.

Product Name : Entadfi

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

December 13, 2021

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Details:

Finasteride and tadalafil combination is used to treat men with benign prostatic hyperplasia (BPH). Tadalafil is a PDE5 inhibitor and finasteride blocks the action of 5-alpha-reductase which will increase testosterone levels in the body, which decreases prostate size.


Lead Product(s): Finasteride,Tadalafil

Therapeutic Area: Urology Brand Name: Finasteride/Tadalafil-Generic

Study Phase: Approved FDFProduct Type: Other Small Molecule

Sponsor: Inapplicable

Deal Size: Inapplicable Upfront Cash: Inapplicable

Deal Type: Inapplicable October 26, 2021

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06

Prague Scientific

Czech Republic
arrow
Pharmex
Not Confirmed

Prague Scientific

Czech Republic
arrow
Pharmex
Not Confirmed

Details : Finasteride and tadalafil combination is used to treat men with benign prostatic hyperplasia (BPH). Tadalafil is a PDE5 inhibitor and finasteride blocks the action of 5-alpha-reductase which will increase testosterone levels in the body, which decreases ...

Product Name : Finasteride/Tadalafil-Generic

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

October 26, 2021

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Details:

Under the terms of the licensing agreement, Hikma will be responsible for the registration and commercialisation of the product Finjuve, in certain MENA markets and Almirall will be responsible for product supply.


Lead Product(s): Finasteride

Therapeutic Area: Dermatology Brand Name: Finjuve

Study Phase: Approved FDFProduct Type: Other Small Molecule

Sponsor: Hikma Pharmaceuticals

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement January 11, 2021

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Almirall

Spain
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Pharmex
Not Confirmed

Almirall

Spain
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Details : Under the terms of the licensing agreement, Hikma will be responsible for the registration and commercialisation of the product Finjuve, in certain MENA markets and Almirall will be responsible for product supply.

Product Name : Finjuve

Product Type : Other Small Molecule

Upfront Cash : Undisclosed

January 11, 2021

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Europe

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Helvepharm AG

France
  • fda
  • EDQM
  • WHO-GMP

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Regulatory Info :

Registration Country : Switzerland

Finasteride

Brand Name : Finasteride Zentiva

Dosage Form : Filmtabl

Dosage Strength : 5mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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02

Helvepharm AG

France
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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Regulatory Info :

Registration Country : Switzerland

Finasteride

Brand Name : Finasteride Zentiva

Dosage Form : Filmtabl

Dosage Strength : 5mg

Packaging :

Approval Date :

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Registration Country : Switzerland

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finasteride

Brand Name : Finasteride Orion

Dosage Form : FILM COATED PILL

Dosage Strength : 5 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

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Regulatory Info : Registered in EU

Registration Country : Germany

Finasteride

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Registered in EU

Registration Country : Germany

Tiefenbacher Compnay Banner

05

  • fda
  • EDQM
  • WHO-GMP

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Regulatory Info : Registered in EU

Registration Country : Germany

Finasteride

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 1MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Registered in EU

Registration Country : Germany

Tiefenbacher Compnay Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

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Regulatory Info :

Registration Country : Italy

Finasteride

Brand Name : FINASTERIDE THINK

Dosage Form : Film-Coated Tablets

Dosage Strength : 5 mg

Packaging : 15 UNITS 5 MG - ORAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Towa Pharmaceutical

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

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Regulatory Info :

Registration Country : Italy

Finasteride

Brand Name : FINASTERIDE THINK

Dosage Form : Film-Coated Tablets

Dosage Strength : 5 mg

Packaging : 30 UNITS 5 MG - ORAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

Towa Pharmaceutical

08

Pharmex
Not Confirmed
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Pharmex
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Finasteride

Brand Name : Finasteride

Dosage Form : Finasteride 5Mg 15 Units Oral Use

Dosage Strength : 15 cpr riv 5 mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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Pharmex
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Finasteride

Brand Name : FINASTERIDE DOC

Dosage Form : Film-Coated Tablets

Dosage Strength : 5 mg

Packaging : 15 UNITS 5 MG - ORAL USE

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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Country
Pharmex
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Finasteride

Brand Name : 28 Arahormo 5Mg Film-Coated Tablets Efg

Dosage Form : Film Coated Tablet

Dosage Strength : 5 Mg/Film Coated Tablet

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Spain

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Listed Dossiers

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  • WHO-GMP

Virtual BoothOctavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.

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Regulatory Info :

Registration Country : India

Finasteride

Brand Name : Finasteride

Dosage Form : DC Granules

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Octavius Pharma

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothOctavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.

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Packaging :

Regulatory Info :

Finasteride

Dosage : DC Granules

Dosage Strength : 5MG

Brand Name : Finasteride

Approval Date :

Application Number :

Registration Country : India

Octavius Pharma

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWe are the TIEFENBACHER GROUP, Health Pioneers since 1963.

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Regulatory Info : Registered in EU

Registration Country : Germany

Finasteride

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Registered in EU

Registration Country : Germany

Tiefenbacher Compnay Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWe are the TIEFENBACHER GROUP, Health Pioneers since 1963.

Flag Germany
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Packaging :

Regulatory Info : Registered in EU

Finasteride

Dosage : Film Coated Tablet

Dosage Strength : 5MG

Brand Name :

Approval Date :

Application Number :

Registration Country : Germany

Tiefenbacher Compnay Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWe are the TIEFENBACHER GROUP, Health Pioneers since 1963.

Flag Germany
Digital Content Digital Content

Regulatory Info : Registered in EU

Registration Country : Germany

Finasteride

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 1MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : Registered in EU

Registration Country : Germany

Tiefenbacher Compnay Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWe are the TIEFENBACHER GROUP, Health Pioneers since 1963.

Flag Germany
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Packaging :

Regulatory Info : Registered in EU

Finasteride

Dosage : Film Coated Tablet

Dosage Strength : 1MG

Brand Name :

Approval Date :

Application Number :

Registration Country : Germany

Tiefenbacher Compnay Banner

04

Pharmathen SA

Greece
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

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Regulatory Info : EU Approved

Registration Country : Greece

Finasteride

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info : EU Approved

Registration Country : Greece

Pharmathen

04

Pharmathen SA

Greece
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

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Packaging :

Regulatory Info : EU Approved

Finasteride

Dosage : Film Coated Tablet

Dosage Strength : 5MG

Brand Name :

Approval Date :

Application Number :

Registration Country : Greece

Pharmathen

05

Pharmex
Not Confirmed
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Not Confirmed

Finasteride

Brand Name : Dilaprost

Dosage Form : FC Tablet

Dosage Strength : 1MG

Packaging : 100 Film Coated Tablet / Box

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Turkey

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Pharmex
Not Confirmed
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Finasteride

Dosage : FC Tablet

Dosage Strength : 1MG

Brand Name : Dilaprost

Approval Date :

Application Number :

Registration Country : Turkey

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Grupo Azevedos

Portugal
Pharmex
Not Confirmed
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Grupo Azevedos

Portugal
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Pharmex
Not Confirmed

Finasteride

Brand Name :

Dosage Form : Film-coated tablets

Dosage Strength : 5MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Portugal

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Grupo Azevedos

Portugal
Pharmex
Not Confirmed
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Grupo Azevedos

Portugal
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Not Confirmed

Finasteride

Dosage : Film-coated tablets

Dosage Strength : 5MG

Brand Name :

Approval Date :

Application Number :

Registration Country : Portugal

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Pharmex
Not Confirmed
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Finasteride

Brand Name :

Dosage Form : Film Coated Tablet

Dosage Strength : 1MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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Pharmex
Not Confirmed
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Finasteride

Dosage : Film Coated Tablet

Dosage Strength : 1MG

Brand Name :

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Application Number :

Registration Country : India

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Pharmex
Not Confirmed
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Finasteride

Brand Name :

Dosage Form : Coated IR Pellets

Dosage Strength : 6.5%/W/W

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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Pharmex
Not Confirmed
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Finasteride

Dosage : Coated IR Pellets

Dosage Strength : 6.5%/W/W

Brand Name :

Approval Date :

Application Number :

Registration Country : India

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Pharmex
Not Confirmed
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Finasteride

Brand Name : FINA/GROWVITA-1

Dosage Form : Tablet

Dosage Strength : 1mg

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

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Pharmex
Not Confirmed
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Not Confirmed

Finasteride

Dosage : Tablet

Dosage Strength : 1mg

Brand Name : FINA/GROWVITA-1

Approval Date :

Application Number :

Registration Country : India

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Pharmex
Not Confirmed
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Pharmex
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Finasteride

Brand Name :

Dosage Form : Tablet

Dosage Strength : 1MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : China

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Pharmex
Not Confirmed
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Finasteride

Dosage : Tablet

Dosage Strength : 1MG

Brand Name :

Approval Date :

Application Number :

Registration Country : China

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DRUG PRODUCT COMPOSITIONS

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DOSAGE - TABLET;ORAL - 5MG

USFDA APPLICATION NUMBER - 20180

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DOSAGE - TABLET;ORAL - 1MG

USFDA APPLICATION NUMBER - 20788

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ABOUT THIS PAGE

Looking for 98319-26-7 / Finasteride API manufacturers, exporters & distributors?

Finasteride manufacturers, exporters & distributors 1

54

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

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

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

API | Excipient name

Finasteride

Synonyms

98319-26-7, Proscar, Propecia, Finastid, Prostide, Chibro-proscar

Cas Number

98319-26-7

Unique Ingredient Identifier (UNII)

57GNO57U7G

About Finasteride

An orally active 3-OXO-5-ALPHA-STEROID 4-DEHYDROGENASE inhibitor. It is used as a surgical alternative for treatment of benign PROSTATIC HYPERPLASIA.

Finasteride (Proscar) Manufacturers

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

Finasteride (Proscar) Suppliers

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

click here to find a list of Finasteride (Proscar) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Finasteride (Proscar) USDMF

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

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

click here to find a list of Finasteride (Proscar) suppliers with USDMF on PharmaCompass.

Finasteride (Proscar) 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 Finasteride (Proscar) Drug Master File in Japan (Finasteride (Proscar) JDMF) empowers Finasteride (Proscar) 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 Finasteride (Proscar) JDMF during the approval evaluation for pharmaceutical products. At the time of Finasteride (Proscar) 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 Finasteride (Proscar) suppliers with JDMF on PharmaCompass.

Finasteride (Proscar) KDMF

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

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

After submitting a Finasteride (Proscar) 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 Finasteride (Proscar) API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Finasteride (Proscar) suppliers with KDMF on PharmaCompass.

Finasteride (Proscar) CEP

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

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

Finasteride (Proscar) WC

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

click here to find a list of Finasteride (Proscar) suppliers with Written Confirmation (WC) on PharmaCompass.

Finasteride (Proscar) 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 Finasteride (Proscar) as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Finasteride (Proscar) 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 Finasteride (Proscar) 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 Finasteride (Proscar) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Finasteride (Proscar) NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Finasteride (Proscar) suppliers with NDC on PharmaCompass.

Finasteride (Proscar) GMP

Finasteride (Proscar) 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 Finasteride (Proscar) 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 Finasteride (Proscar) GMP manufacturer or Finasteride (Proscar) GMP API supplier for your needs.

Finasteride (Proscar) CoA

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

Finasteride (Proscar) CoA mostly includes findings from lab analyses of a specific batch. For each Finasteride (Proscar) 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.

Finasteride (Proscar) may be tested according to a variety of international standards, such as European Pharmacopoeia (Finasteride (Proscar) EP), Finasteride (Proscar) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Finasteride (Proscar) 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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