Synopsis
Synopsis
0
VMF
DRUG PRODUCT COMPOSITIONS0
Weekly News Recap #Phispers
1. Cialis
2. Ic 351
3. Ic-351
4. Ic351
5. Pyrazino(1',2':1,6)pyrido(3,4-b)indole-1,4-dione, 6-(1,3- Benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methyl-, (6r,12ar)-
1. Cialis
2. 171596-29-5
3. Ic351
4. Tadanafil
5. Adcirca
6. Ic 351
7. Icos 351
8. Ic-351
9. Gf 196960
10. (6r,12ar)-6-(benzo[d][1,3]dioxol-5-yl)-2-methyl-2,3,12,12a-tetrahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4(6h,7h)-dione
11. Tadalafil Mylan
12. Trans-tadalafil
13. Tadalafil(cialis)
14. (6r,12ar)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-(methylenedioxy)phenyl) Pyrazino(1',2':1,6)pyrido(3,4-b)indole-1,4-dione
15. (6r-trans)-6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methyl-pyrazino(1',2':1,6)pyrido(3,4-b)indole-1,4-dione
16. Chembl779
17. Nsc-750236
18. Nsc-759172
19. 742sxx0ict
20. Gf-196960
21. Ly-450190
22. (6r,12ar)-6-(benzo[d][1,3]dioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione
23. Chebi:71940
24. Tadalafil [usan]
25. Ly450190
26. Dsstox_cid_26786
27. Dsstox_rid_81904
28. Dsstox_gsid_46786
29. (6r,12ar)-6-(1,3-benzodioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione
30. 6-benzo[1,3]dioxol-5-yl-2-methyl-2,3,6,7,12,12a-hexahydro-pyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione
31. Tadalafil Lilly
32. Smr000466321
33. Cialis (tn)
34. Tildenafil
35. Cas-171596-29-5
36. Hsdb 7303
37. Unii-742sxx0ict
38. Tadalafila
39. Tadalafilo
40. Taldalafil
41. Tadalafil [usan:inn:ban]
42. Tadalafil Solution
43. 1xoz
44. Cialis, Tadalafil
45. Ncgc00168781-01
46. Tadalafil- Bio-x
47. (2r,8r)-2-(1,3-benzodioxol-5-yl)-6-methyl-3,6,17-triazatetracyclo[8.7.0.0^{3,8}.0^{11,16}]heptadeca-1(10),11,13,15-tetraene-4,7-dione
48. Adcirca (tn)
49. Tadalafil (cialis)
50. Zalutia (tn)
51. (6r,12ar)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylenedioxyphenyl)pyrazino(1',2':1,6)pyrido(3,4-b)indole-1,4-dione
52. Ks-1117
53. Tadalafil [inn]
54. Tadalafil [jan]
55. Tadalafil [mi]
56. Tadalafil; Cialis
57. Tadalafil [hsdb]
58. Tadalafil [vandf]
59. (-)-tadalafil (6r)
60. Tadalafil [mart.]
61. Tadalafil [usp-rs]
62. Tadalafil [who-dd]
63. Tadalafil (jan/usp/inn)
64. Schembl33333
65. Tadalafil [ema Epar]
66. Mls000759426
67. Mls001165782
68. Mls001195644
69. Mls001424132
70. Mls006010126
71. Tadalafil Specified Impurity A
72. Gtpl7299
73. Tadalafil [orange Book]
74. Dtxsid9046786
75. Tadalafil [ep Monograph]
76. Bdbm14777
77. Tadalafil (6r ,12as)- Lilly
78. Tadalafil [usp Monograph]
79. Entadfi Component Tadalafil
80. Hms2051n17
81. Hms2235l21
82. Hms3884g19
83. Pharmakon1600-01505639
84. Amy10321
85. Ex-a2644
86. Zinc3993855
87. Tox21_112642
88. Hy-90009a
89. Mfcd07771966
90. Nsc750236
91. Nsc759172
92. S1512
93. Tadalafil 1.0 Mg/ml In Acetonitrile
94. Tadalafil 100 Microg/ml In Methanol
95. Tadalafil Component Of Entadfi
96. Akos015892559
97. Tox21_112642_1
98. Ab42193
99. Ccg-100973
100. Cs-1414
101. Db00820
102. Nc00223
103. Nsc 750236
104. Nsc 759172
105. 1,3-benzodioxol-5-yl(methyl)[?]dione
106. Ncgc00263909-02
107. Tadalafil 100 Microg/ml In Acetonitrile
108. (6r,12ar)-6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methylpyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione
109. Bt164435
110. Gf196960
111. Pyrazino(1',2':1,6)pyrido(3,4-b)indole-1,4-dione, 6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methyl-, (6r,12ar)-
112. Pyrazino(1',2':1,6)pyrido(3,4-b)indole-1,4-dione, 6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methyl-, (6r-trans)-
113. (-)-tadalafil (6r ,12as) Diastereomer
114. Sw197603-2
115. A23556
116. D02008
117. Ab00639969-08
118. Ab00639969_09
119. Ab00639969_10
120. 596t295
121. Ar-270/43507798
122. Q424156
123. Sr-05000001940
124. Sr-05000001940-1
125. Brd-k93645900-001-04-8
126. Tadalafil Solution, 1.0 Mg/ml In Acetonitrile, Ampule Of 1 Ml, Certified Reference Material
127. (2r,8r)-2-(1,3-benzodioxol-5-yl)-6-methyl-3,6,17-triazatetracyclo[8.7.0.03,8.011,16]heptadeca-1(10),11,13,15-tetraene-4,7-dione
128. (2r,8r)-2-(2h-1,3-benzodioxol-5-yl)-6-methyl-3,6,17-triazatetracyclo[8.7.0.0^{3,8}.0^{11,16}]heptadeca-1(10),11(16),12,14-tetraene-4,7-dione
129. (2r,8r)-2-(2h-1,3-benzodioxol-5-yl)-6-methyl-3,6,17-triazatetracyclo[8.7.0.0^{3,8}.0^{11,16}]heptadeca-1(10),11,13,15-tetraene-4,7-dione
130. (6r,12 Ar)-6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methylpyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione
131. (6r,12ar) 6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methylpyrazino [1',2':1,6] Pyrido[3,4-b]indole-1,4-dione
132. (6r,12ar) 6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methylpyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione
133. (6r,12ar)-6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methylpyrazino[1,2:1,6]pyrido[3,4-b]indole-1,4-dione
134. (6r,12ar)-6-(1,3-benzodioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[1,2,1,6]pyrido[3,4-b]indole-1,4-dione
135. (6r,3,6,7,12,12a-hexahydro-2-methyl-6-[3,4-(methylenedioxy)phenyl]pyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione
136. 1242099-07-5
137. 171488-03-2
138. 6-(1,3-benzodioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[2',1':6,1]pyrido[3,4-b]indole-1,4-dione
139. Pyrazino(1',2':1,6)pyrido(3,4-b)indole-1,4-dione, 6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methyl-, (6r-12ar)-
140. Pyrazino[1',6]pyrido[3,4-b]indole-1,4-dione, 6-(1,3-benzodioxol-5-yl)-2,3,6,7,12,12ahexahydro-2-methyl-, (6r,12ar)-
141. Rel-(6r,12ar)-6-(benzo[d][1,3]dioxol-5-yl)-2-methyl-2,3,12,12a-tetrahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4(6h,7h)-dione
| Molecular Weight | 389.4 g/mol |
|---|---|
| Molecular Formula | C22H19N3O4 |
| XLogP3 | 2.3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 389.13755610 g/mol |
| Monoisotopic Mass | 389.13755610 g/mol |
| Topological Polar Surface Area | 74.9 Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 702 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
| 1 of 6 | |
|---|---|
| Drug Name | Adcirca |
| PubMed Health | Tadalafil (By mouth) |
| Drug Classes | Antihypertensive, Erectile Dysfunction Agent |
| Drug Label | ADCIRCA (tadalafil), an oral treatment for pulmonary arterial hypertension, is a selective inhibitor of cyclic guanosine monophosphate (cGMP)specific phosphodiesterase type 5 (PDE5). Tadalafil has the empirical formula C22H19N3O4 representing a mo... |
| Active Ingredient | Tadalafil |
| Dosage Form | Tablet |
| Route | Oral |
| Strength | 20mg |
| Market Status | Prescription |
| Company | Eli Lilly |
| 2 of 6 | |
|---|---|
| Drug Name | Cialis |
| PubMed Health | Tadalafil (By mouth) |
| Drug Classes | Antihypertensive, Erectile Dysfunction Agent |
| Drug Label | CIALIS (tadalafil) is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5). Tadalafil has the empirical formula C22H19N3O4 representing a molecular weight of 389.41. The structural formula is: The ch... |
| Active Ingredient | Tadalafil |
| Dosage Form | Tablet |
| Route | Oral |
| Strength | 2.5mg; 5mg; 10mg; 20mg |
| Market Status | Prescription |
| Company | Lilly |
| 3 of 6 | |
|---|---|
| Drug Name | Tadalafil |
| PubMed Health | Tadalafil (By mouth) |
| Drug Classes | Antihypertensive, Erectile Dysfunction Agent |
| Drug Label | CIALIS (tadalafil) is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5). Tadalafil has the empirical formula C22H19N3O4 representing a molecular weight of 389.41. The structural formula is: The ch... |
| Active Ingredient | Tadalafil |
| Dosage Form | Tablet |
| Route | oral |
| Strength | 20mg |
| Market Status | Tentative Approval |
| Company | Synthon Pharms |
| 4 of 6 | |
|---|---|
| Drug Name | Adcirca |
| PubMed Health | Tadalafil (By mouth) |
| Drug Classes | Antihypertensive, Erectile Dysfunction Agent |
| Drug Label | ADCIRCA (tadalafil), an oral treatment for pulmonary arterial hypertension, is a selective inhibitor of cyclic guanosine monophosphate (cGMP)specific phosphodiesterase type 5 (PDE5). Tadalafil has the empirical formula C22H19N3O4 representing a mo... |
| Active Ingredient | Tadalafil |
| Dosage Form | Tablet |
| Route | Oral |
| Strength | 20mg |
| Market Status | Prescription |
| Company | Eli Lilly |
| 5 of 6 | |
|---|---|
| Drug Name | Cialis |
| PubMed Health | Tadalafil (By mouth) |
| Drug Classes | Antihypertensive, Erectile Dysfunction Agent |
| Drug Label | CIALIS (tadalafil) is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5). Tadalafil has the empirical formula C22H19N3O4 representing a molecular weight of 389.41. The structural formula is: The ch... |
| Active Ingredient | Tadalafil |
| Dosage Form | Tablet |
| Route | Oral |
| Strength | 2.5mg; 5mg; 10mg; 20mg |
| Market Status | Prescription |
| Company | Lilly |
| 6 of 6 | |
|---|---|
| Drug Name | Tadalafil |
| PubMed Health | Tadalafil (By mouth) |
| Drug Classes | Antihypertensive, Erectile Dysfunction Agent |
| Drug Label | CIALIS (tadalafil) is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5). Tadalafil has the empirical formula C22H19N3O4 representing a molecular weight of 389.41. The structural formula is: The ch... |
| Active Ingredient | Tadalafil |
| Dosage Form | Tablet |
| Route | oral |
| Strength | 20mg |
| Market Status | Tentative Approval |
| Company | Synthon Pharms |
Tadalafil is indicated for the treatment of erectile dysfunction. /Included in US product labeling/
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
The Food and Drug Administration ... approved updated labeling for Cialis, Levitra and Viagra to reflect a small number of post-marketing reports of sudden vision loss, attributed to NAION (non arteritic ischemic optic neuropathy), a condition where blood flow is blocked to the optic nerve. FDA advises patients to stop taking these medicines, and call a doctor or healthcare provider right away if they experience sudden or decreased vision loss in one or both eyes. Further, patients taking or considering taking these products should inform their health care professionals if they have ever had severe loss of vision, which might reflect a prior episode of NAION. Such patients are at an increased risk of developing NAION again.
US FDA; FDA Statement. FDA Updates Labeling for Viagra, Cialis and Levitra for Rare Post-Marketing Reports of Eye Problems (July 8, 2005) Available from, as of July 12, 2005: https://www.fda.gov/bbs/topics/NEWS/2005/NEW01201.html
Cardiovascular status of patients should be considered since there is a degree of risk associated with sexual activity; treatments for erectile dysfunction, including tadalafil, should not be used in men for whom sexual activity is inadvisable as a result of their underlying cardiac status.
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
The following groups of patients with cardiovascular disease were not included in clinical safety and efficacy trials for Cialis, and, therefore, the use of Cialis is not recommended in these groups until further information is available: patients with a myocardial infarction within the last 90 days, patients with unstable angina or angina occurring during sexual intercourse, patients with New York Heart Association Class 2 or greater heart failure in the last 6 months, patients with uncontrolled arrhythmias, hypotension (<90/50 mm Hg), or uncontrolled hypertension (>170/100 mm Hg), and patients with a stroke within the last 6 months. In addition, patients with known hereditary degenerative retinal disorders, including retinitis pigmentosa, were not included in the clinical trials, and use in these patients is not recommended.
Physicians Desk Reference. 58th ed. Thomson PDR. Montvale, NJ 2004.
The effect of a 100 mg single dose of tadalafil on the QT interval was evaluated at the time of peak tadalafil concentration in a randomized, double-blinded, placebo, and active (intravenous ibutilide)-controlled crossover study in 90 healthy males aged 18 to 53 years. The mean change in QTc (Fridericia QT correction) for tadalafil, relative to placebo, was 3.5 milliseconds (two-sided 90% CI=1.9, 5.1). The mean change in QTc (Individual QT correction) for tadalafil, relative to placebo, was 2.8 milliseconds (two-sided 90% CI=1.2, 4.4). A 100 mg dose of tadalafil (5 times the highest recommended dose) was chosen because this dose yields exposures covering those observed upon coadministration of tadalafil with potent CYP3A4 inhibitors or those observed in renal impairment. In this study, the mean increase in heart rate associated with /this/ dose of tadalafil compared to placebo was 3.1 beats per minute.
Physicians Desk Reference. 58th ed. Thomson PDR. Montvale, NJ 2004.
For more Drug Warnings (Complete) data for TADALAFIL (18 total), please visit the HSDB record page.
Tadalafil is indicated for the treatment of erectile dysfunction (ED) and either alone or in combination with [finasteride] for the treatment of benign prostatic hypertrophy (BPH). It is also indicated for the treatment of pulmonary arterial hypertension (PAH) both alone and in combination with [macitentan] or other endothelin-1 antagonists.
FDA Label
Adcirca is indicated in adults for the treatment of pulmonary arterial hypertension (PAH) classified as World Health Organization functional class II and III, to improve exercise capacity (see section 5. 1).
Efficacy has been shown in idiopathic PAH (IPAH) and in PAH related to collagen vascular disease.
Treatment of erectile dysfunction.
In order for tadalafil to be effective, sexual stimulation is required.
Cialis is not indicated for use by women.
Treatment of erectile dysfunction in adult males.
In order for tadalafil to be effective, sexual stimulation is required.
Tadalafil Lilly is not indicated for use by women.
Treatment of the signs and symptoms of benign prostatic hyperplasia in adult males.
Treatment of erectile dysfunction in adult males.
In order for tadalafil to be effective, sexual stimulation is required.
Tadalafil Mylan is not indicated for use by women.
Talmanco is indicated in adults for the treatment of pulmonary arterial hypertension (PAH) classified as WHO functional class II and III, to improve exercise capacity. Efficacy has been shown in idiopathic PAH (IPAH) and in PAH related to collagen vascular disease.
Treatment of pulmonary arterial hypertension
Tadalafil exerts a therapeutic effect in ED by increasing sexual stimulation-dependant smooth muscle relaxation in the penis, allowing the corpus cavernosum to fill with blood to produce an erection. Smooth muscle relaxation in the pulmonary vasculature helps to produce vasodilation in PAH which reduces blood pressure in the pulmonary arteries. In BPH, tadalafil may contribute to decreased smooth muscle cell proliferation which may reduce the size of the prostate and relieve the anatomical obstruction which produces urinary symptoms of BPH. The decreased affinity of tadalafil for PDE6 compared to other PDE5 inhibitors may explain the reduced incidence of visual side effects.
Vasodilator Agents
Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)
Phosphodiesterase 5 Inhibitors
Compounds that specifically inhibit PHOSPHODIESTERASE 5. (See all compounds classified as Phosphodiesterase 5 Inhibitors.)
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.)
G04BE08
G04BE08
G04BE08
G04BE08
G04BE08
G04BE08
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
G - Genito urinary system and sex hormones
G04 - Urologicals
G04B - Urologicals
G04BE - Drugs used in erectile dysfunction
G04BE08 - Tadalafil
Absorption
Tadalafil has a tmax of 0.5-6h with a median of 2h in healthy adults. The tmax in adults with PAH is reported as 2-8h with a median of 4h. There does not appear to be a significant effect on absorption when tadalafil is taken with food.
Route of Elimination
Tadalafil is primarily eliminated via hepatic metabolism. These metabolites are mainly excreted in the feces (61%) and to a lesser extent in the urine (36%)
Volume of Distribution
Tadalafil has a mean apparent volume of distribution of 63L in healthy adults. The mean apparent volume of distribution is reported as 77L in adults with PAH.
Clearance
The mean apparent oral clearance of tadalafil is 2.5-3.4L/h in healthy adults. The mean apparent oral clearance in adults with PAH is reported as 3.5L/h
Tmax: 30 minutes to 6 hours (median 2 hours). Absolute bioavailability has not been determined; rate and extent of absorption are not influenced by food.
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
Volume of distribution: 63 L; indicating distribution into tissues. Less than 0.0005% of administered dose was found in the semen of healthy subjects. 94% protein bound.
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
Over a dose range of 2.5 to 20 mg, tadalafil exposure (AUC) increases proportionally with dose in healthy subjects. Steady-state plasma concentrations are attained within 5 days of once-daily dosing, and exposure is approximately 1.6-fold greater than after a single dose.
Physicians Desk Reference. 58th ed. Thomson PDR. Montvale, NJ 2004.
Elimination: Mean oral clearance: 2.5 L per hour. Fecal: 61%. Urine: 36%.
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
For more Absorption, Distribution and Excretion (Complete) data for TADALAFIL (11 total), please visit the HSDB record page.
Tadalafil undergoes hepatic metabolism via CYP3A4 to a catechol metabolite. This catechol metabolite undergoes subsequent methylation and glucuronidation with the methyl-glucuronide metabolite becoming the primary metabolite in circulation. None of the known metabolites are considered to be active.
Biotransformation: Hepatic metabolism, mainly by CYP3A4. Tadalafil is predominantly metabolized by CYP3A4 to a catechol metabolite. The catechol metabolite undergoes extensive methylation and glucuronidation to form the methylcatechol and methylcatechol glucuronide conjugate, respectively. The major circulating metabolite is the methylcatechol glucuronide. Methylcatechol concentrations are less than 10% of glucuronide concentrations. In vitro data suggests that metabolites are not expected to be pharmacologically active at observed metabolite concentrations.
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
The mean half-life of elimination of tadalafil is 15-17.5h in healthy adults. The mean half-life of elimination in adults with PAH is reported as 35h.
Terminal: 17.5 hours
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
Tadalafil is a selective phosphodiesterase-5 (PDE5) inhibitor that produces several downstream effects with the most common therapeutic effect being smooth muscle relaxation. Patients may experience ED due to a variety of causes including psychogenic, neurogenic, vasculogenic, iatrogenic, or endocrine. These causes result in dysfunction of penile smooth muscle relaxation through either disrupted neuronal signaling or direct influence on smooth muscle cells. During sexual arousal, non-adrenergic non-cholinergic (NANC) neurons release nitric oxide (NO). Nitric oxide stimulates guanylate cyclase which converts guanosine triphosphate to cyclic guanosine monophosphate (cGMP). cGMP activates the cGMP-dependent kinase (PKG) in a signal cascade which activates K+ channels leading to inhibition of Ca2+ channels, inhibits platelet activation, and inhibits smooth muscle cell proliferation while inducing apoptosis. This signal cascade is attenuated by PDE5 which breaks the phosphodiester bond of cGMP, converting it to GMP. Inhibition of PDE5 by tadalafil increases signaling via the PKG cascade which supports penile smooth muscle relaxation during sexual arousal by decreasing Ca2+ entry into smooth muscle cells. This smooth muscle relaxation allows blood to fill the corpus cavernosum thereby producing an erection. In PAH, blood pressure in the pulmonary arteries is raised due to a variety of mechanisms stemming from endothelial dysfunction. Decreased production of NO and prostacyclin reduce vasodilatory signaling while overproduction of endothelin-1 and thromboxane increase vasoconstriction. Inflammation, thromboses, and hypoxia later contribute to vascular remodeling which further reduces luminal size. The resultant increase in blood pressure reduces the capacity for gas exchange and increases afterload at the right ventricle, producing symptoms of dyspnea, fatigue, and dizziness as well as leading to right-sided heart failure. Tadalafil exerts its therapeutic effect in PAH through boosting NO-cGMP signaling to contribute to smooth muscle relaxation as with ED. Lastly, tadalafil is used to treat BPH. BPH produces urinary dysfunction through hyperproliferation of the epithelial and smooth muscle layers of the prostate. The increased size of the prostate blocks urine flow through the urethra resulting in higher residual volumes due to incomplete emptying. Tadalafil does not appear to exert its benefit via smooth muscle relaxation of the prostate. It may instead exert its effect through a mix of increased oxygenation and decreased inflammation, which decreases tissue remodeling, and inhibition of cell proliferation through the cGMP cascade. The decreased affinity for PDE6 compared to other PDE5 inhibitors may explain the decreased incidence of visual side effects as PDE6 is present in the eye and contributes to color vision.
In vitro studies have shown that the effect of tadalafil is more potent on phosphodiesterase type 5 (PDE5) than on other phosphodiesterases. These studies have shown that tadalafil is >10,000-fold more potent for PDE5 than for PDE1, PDE2, PDE4, and PDE7 enzymes, which are found in the heart, brain, blood vessels, liver, leukocytes, skeletal muscle, and other organs. Tadalafil is >10,000-fold more potent for PDE5 than for PDE3, an enzyme found in the heart and blood vessels. Additionally, tadalafil is 700-fold more potent for PDE5 than for PDE8, PDE9, PDE10 and 14-fold more potent for PDE5 than for PDE11A1, an enzyme found in human skeletal muscle. Tadalafil inhibits human recombinant PDE11A1 activity at concentrations within the therapeutic range. The physiological role and clinical consequence of PDE11 inhibition in humans have not been defined.
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
Studies in vitro have demonstrated that tadalafil is a selective inhibitor of phosphodiesterase type 5 (PDE5). PDE5 is found in corpus cavernosum smooth muscle, vascular and visceral smooth muscle, skeletal muscle, platelets, kidney, lung, cerebellum, and pancreas.
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
Penile erection during sexual stimulation is caused by increased penile blood flow resulting from the relaxation of penile arteries and corpus cavernosum smooth muscle. This response is mediated by the release of nitric oxide (NO) from nerve terminals and endothelial cells, which stimulates the synthesis of cyclic GMP in smooth muscle cells. Cyclic GMP causes smooth muscle relaxation and increased blood flow into the corpus cavernosum. The inhibition of phosphodiesterase type 5 (PDE5) enhances erectile function by increasing the amount of cyclic GMP. Tadalafil inhibits PDE5. Because sexual stimulation is required to initiate the local release of nitric oxide, the inhibition of PDE5 by tadalafil has no effect on the absence of sexual stimulation.
Thomson.Micromedex. Drug Information for the Health Care Professional. 24th ed. Volume 1. Plus Updates. Content Reviewed by the United States Pharmacopeial Convention, Inc. Greenwood Village, CO. 2004.
API SUPPLIERS
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USDMF
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
GDUFA
DMF Review : Complete
Rev. Date : 2018-03-07
Pay. Date : 2017-11-15
DMF Number : 24590
Submission : 2011-01-31
Status : Active
Type : II
AMI Lifesciences is Driven by Chemistry. Powered by People.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37995
Submission : 2023-02-10
Status : Active
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2016-07-28
Pay. Date : 2016-07-18
DMF Number : 20884
Submission : 2007-09-26
Status : Active
Type : II
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
GDUFA
DMF Review : Complete
Rev. Date : 2016-02-08
Pay. Date : 2015-09-29
DMF Number : 29765
Submission : 2015-12-04
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-22
Pay. Date : 2012-11-02
DMF Number : 22707
Submission : 2009-03-31
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22530
Submission : 2009-02-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20962
Submission : 2007-10-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-12-04
Pay. Date : 2014-11-13
DMF Number : 24206
Submission : 2010-09-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22771
Submission : 2009-05-13
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-10-31
Pay. Date : 2013-08-27
DMF Number : 20640
Submission : 2007-06-15
Status : Active
Type : II
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Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
NDC Package Code : 12658-0439
Start Marketing Date : 2003-11-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
NDC Package Code : 62128-0385
Start Marketing Date : 2003-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
AMI Lifesciences is Driven by Chemistry. Powered by People.
NDC Package Code : 59680-018
Start Marketing Date : 2024-11-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
NDC Package Code : 69037-0015
Start Marketing Date : 2003-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-921
Start Marketing Date : 2015-09-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-719
Start Marketing Date : 2024-01-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72761-017
Start Marketing Date : 2019-03-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-3128
Start Marketing Date : 2017-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 82053-003
Start Marketing Date : 2022-05-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0005
Start Marketing Date : 2011-06-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
About the Company : Interquim, founded in 1978, is now part of the Ferrer HealthTech division. Interquim specializes in the development of competitive processes for manufacturing high added-value APIs...
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
About the Company : Octavius Pharma is a global leader in Directly Compressible Granules with over 45 years of expertise in formulation development, manufacturing, and commercialization. Our portfolio...
Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
About the Company : Century Pharmaceuticals, established in 1982, has 40 years of experience in manufacturing APIs. It has been supplying APIs produced in-house to several major pharma companies in In...
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
About the Company : Polpharma API, part of a leading Polish pharmaceutical group, has over 70 years of experience in process development and cGMP manufacturing. We offer end-to-end solutions, from API...
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, ...
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
About the Company : Gonane Pharma, is a contract pharmaceutical company located in Gujarat, India, specializing in the manufacturing and marketing of Corticosteroids, Hormones, Antivirals, and Oncolog...
Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales was founded in 1999 as an out-of-the-box distribution firm specializing in the global supply of high-quality pharmaceutical ingredients. The firm provides complete ...
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
About the Company : Shandong Chenghui Shuangda Pharmaceutical Co., Ltd. is specialized in R&D and production of APIs and advanced intermediates. With 22 years of production experience,the company has ...
AMI Lifesciences is Driven by Chemistry. Powered by People.
About the Company : Ami Lifesciences, established in 2006, is one of the fastest growing API manufacturing companies in India. Specializing in cardiovascular, anti-diabetic, CNS, and respiratory thera...
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Global is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
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Drugs in Development
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Towa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.
Regulatory Info :
Registration Country : Italy
Brand Name : TADALAFIL THINK
Dosage Form : Film-Coated Tablets
Dosage Strength : 20 mg
Packaging : 12 UNITS 20 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Cialis
Dosage Form :
Dosage Strength : 8 Cpr Riv 20 Mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Brand Name : Cialis
Dosage Form :
Dosage Strength : 4 Cpr Riv 20 Mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Cialis
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 2.5 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Brand Name : Cialis
Dosage Form : Antic-calc Tablet, Film Coated
Dosage Strength : 20 mg
Packaging : Blister
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Generic US CTD
Registration Country : United Kingdom
Brand Name :
Dosage Form : TABLET
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number : 21368
Regulatory Info : Generic US CTD
Registration Country : United Kingdom
Regulatory Info : Generic US CTD
Registration Country : United Kingdom
Brand Name :
Dosage Form : TABLET
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic US CTD
Registration Country : United Kingdom
Regulatory Info :
Registration Country : Sweden
Brand Name : Tadalafil Teva
Dosage Form : FILM COATED PILL
Dosage Strength : 10 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Italy
Brand Name : TADALAFIL MYLAN
Dosage Form : Film-Coated Tablet Oral Use
Dosage Strength : 20 mg
Packaging : 12 UNITS 20 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Generic
Registration Country : Turkey
Brand Name :
Dosage Form : FILM COATED TABLET
Dosage Strength : 10MG
Packaging : 2 Or 4 Or 8 Tablets
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : Turkey
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Canada
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Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Tadalafil
Dosage Form : DC Granules
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Dosage : DC Granules
Dosage Strength : 5MG
Brand Name : Tadalafil
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Tadalafil
Dosage Form : DC Granules
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Dosage : DC Granules
Dosage Strength : 10MG
Brand Name : Tadalafil
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Tadalafil
Dosage Form : DC Granules
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Dosage : DC Granules
Dosage Strength : 20MG
Brand Name : Tadalafil
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Tadalafil
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Dosage : Tablet
Dosage Strength : 5MG
Brand Name : Tadalafil
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Tadalafil
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Dosage : Tablet
Dosage Strength : 10MG
Brand Name : Tadalafil
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Tadalafil
Dosage Form : Tablet
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Dosage : Tablet
Dosage Strength : 20MG
Brand Name : Tadalafil
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Tadalafil; Dapoxetine Hydrochloride
Brand Name : Tadalafil; Dapoxetine ...
Dosage Form : DC Granules
Dosage Strength : 10MG; 30MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Tadalafil; Dapoxetine Hydrochloride
Dosage : DC Granules
Dosage Strength : 10MG; 30MG
Brand Name : Tadalafil; Dapoxetine ...
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Tadalafil; Dapoxetine Hydrochloride
Brand Name : Tadalafil; Dapoxetine ...
Dosage Form : DC Granules
Dosage Strength : 20MG; 60MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Tadalafil; Dapoxetine Hydrochloride
Dosage : DC Granules
Dosage Strength : 20MG; 60MG
Brand Name : Tadalafil; Dapoxetine ...
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Tadalafil; Dapoxetine Hydrochloride
Brand Name : Tadalafil; Dapoxetine ...
Dosage Form : Tablet
Dosage Strength : 10MG; 30MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Tadalafil; Dapoxetine Hydrochloride
Dosage : Tablet
Dosage Strength : 10MG; 30MG
Brand Name : Tadalafil; Dapoxetine ...
Approval Date :
Application Number :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Tadalafil; Dapoxetine Hydrochloride
Brand Name : Tadalafil; Dapoxetine ...
Dosage Form : Tablet
Dosage Strength : 20MG; 60MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Octavius Pharma has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Packaging :
Regulatory Info :
Tadalafil; Dapoxetine Hydrochloride
Dosage : Tablet
Dosage Strength : 20MG; 60MG
Brand Name : Tadalafil; Dapoxetine ...
Approval Date :
Application Number :
Registration Country : India
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - TABLET;ORAL - 10MG
USFDA APPLICATION NUMBER - 21368
DOSAGE - TABLET;ORAL - 2.5MG
USFDA APPLICATION NUMBER - 21368
DOSAGE - TABLET;ORAL - 20MG
USFDA APPLICATION NUMBER - 21368
DOSAGE - TABLET;ORAL - 5MG
USFDA APPLICATION NUMBER - 21368
DOSAGE - TABLET;ORAL - 20MG
USFDA APPLICATION NUMBER - 22332
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Faran Shimi Pharmaceutical
Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
Dosage Form : Tablet
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Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Excipients by Applications
Coating Systems & Additives
Fillers, Diluents & Binders
Controlled & Modified Release
Granulation
Faran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.
Brand Name : Sodium Dodecyl Sulfate
Application : Granulation
Excipient Details : Sodium dodecyl sulfate is used in wet granulation tableting applications for the production of antacid tablets and digestive aids.
Dosage Form : Tablet
Grade : Oral
Category : Granulation, Lubricants & Glidants, Surfactant & Foaming Agents
Brand Name : Sodium Dodecyl Sulfate
Application : Granulation, Lubricants & Glidants, Surfactant & Foaming Agents
Excipient Details : Sodium Dodecyl Sulfate is used as an ionic surfactant, lubricant, and granulating agent in the solid dosage forms such as tablets.
Dosage Form : Tablet
Grade : Oral
Category : Direct Compression, Fillers, Diluents & Binders, Granulation
Application : Direct Compression, Fillers, Diluents & Binders, Granulation
Excipient Details : AceCel is suitable for majority of the directly compressible actives, combines good flow and high compressibility.
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose
Dosage Form : Tablet
Grade : Oral
Category : Direct Compression, Disintegrants & Superdisintegrants, Granulation
Application : Direct Compression, Disintegrants & Superdisintegrants, Granulation
Excipient Details : Croscarmellose sodium, a cellulose-based super disintegrant, provides excellent results in tablet disintegration. It is used in both wet granulation and direct compression.
Dosage Form : Tablet
Grade : Oral
Category : Direct Compression, Fillers, Diluents & Binders, Granulation
Application : Direct Compression, Fillers, Diluents & Binders, Granulation
Excipient Details : HiCel acts as a strong dry binder. It facilitates low tablet friability & promotes rapid tablet disintegration.
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Microcrystalline Cellulose
Application : Fillers, Diluents & Binders, Granulation
Pharmacopoeia Ref : Conforms to USP-NF, Ph.Eur., J...
Technical Specs : Density- Tapped density- 857 g/l, Bulk density- 589 g/l; Particle...
Ingredient(s) : Lactose Monohydrate
Application : Fillers, Diluents & Binders, Granulation
Grade : Not Available
Category : API Stability Enhancers, Coating Systems & Additives, Controlled & Modified Release, Direct Compression, Granulation, Rheology Modifiers, Vegetarian Capsules
Application : API Stability Enhancers, Coating Systems & Additives, Controlled & Modified Release, Direct Compression, Granulation, Rheology Modifiers, Vegetarian Capsules
Excipient Details : Controlled Release, Direct Compression,Wet Granulation,Tablet Coating, Liquid Solutions and Suspensions
Pharmacopoeia Ref : Not Available
Technical Specs : Not Available
Ingredient(s) : Hydroxypropyl Methylcellulose
Dosage Form : Tablet
Grade : Oral
Category : Coating Systems & Additives, Fillers, Diluents & Binders, Granulation
Brand Name : Hydroxypropyl Methyl Cellulose (60E3)
Application : Coating Systems & Additives, Fillers, Diluents & Binders, Granulation
Excipient Details : Hydroxypropyl Methyl Cellulose (60E3) is used as a binding, coating, and granulating agent for the production of tablets.
Application : Granulation
Excipient Details : Wetting agent, reduces disintegration time, Ionic solubilizer, high HLB anionic emulsifier for semi-solids and foams.
Pharmacopoeia Ref : Ph. Eur.: Sodium Laurilsulfate...
Technical Specs : Not Available
Ingredient(s) : Sodium Lauryl Sulfate
Disintegrants & Superdisintegrants
Lubricants & Glidants
Direct Compression
Co-Processed Excipients
Thickeners and Stabilizers
Film Formers & Plasticizers
Taste Masking
Empty Capsules
Rheology Modifiers
Vegetarian Capsules
Coloring Agents
Chewable & Orodispersible Aids
API Stability Enhancers
Emulsifying Agents
Parenteral
Surfactant & Foaming Agents
Solubilizers
Topical
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Global Sales Information
US Medicaid Prescriptions
Company :
Tadalafil
Drug Cost (USD) : 33,526,807
Year : 2022
Prescribers : 906
Prescriptions : 7161
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 6,874,548
Year : 2022
Prescribers : 2187
Prescriptions : 11479
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 103,423,714
Year : 2022
Prescribers : 65301
Prescriptions : 289882
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 43,282,513
Year : 2021
Prescribers : 1172
Prescriptions : 9421
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 8,146,168
Year : 2021
Prescribers : 2728
Prescriptions : 14318
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 103,140,558
Year : 2021
Prescribers : 59582
Prescriptions : 274099
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 11,236,630
Year : 2020
Prescribers : 4127
Prescriptions : 21306
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 55,942,543
Year : 2020
Prescribers : 1609
Prescriptions : 12365
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 94,870,769
Year : 2020
Prescribers : 57729
Prescriptions : 278310
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Company :
Tadalafil
Drug Cost (USD) : 82,753,859
Year : 2019
Prescribers : 2802
Prescriptions : 18903
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Market Place
Patents & EXCLUSIVITIES
US Patents
Patent Expiration Date : 2038-12-24
US Patent Number : 11666576
Drug Substance Claim :
Drug Product Claim : Y
Application Number : 214522
Patent Use Code : U-3397
Delist Requested :
Patent Use Description :
Patent Expiration Date : 2038-12-24
Patent Expiration Date : 2038-12-24
US Patent Number : 11382917
Drug Substance Claim :
Drug Product Claim : Y
Application Number : 214522
Patent Use Code : U-3397
Delist Requested :
Patent Use Description :
Patent Expiration Date : 2038-12-24
Patent Expiration Date : 2038-12-24
US Patent Number : 12186322
Drug Substance Claim :
Drug Product Claim : Y
Application Number : 214522
Patent Use Code : U-3397
Delist Requested :
Patent Use Description :
Patent Expiration Date : 2038-12-24
Patent Expiration Date : 2038-12-24
US Patent Number : 11975006
Drug Substance Claim :
Drug Product Claim : Y
Application Number : 214522
Patent Use Code : U-3397
Delist Requested :
Patent Use Description :
Patent Expiration Date : 2038-12-24
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]REF. STANDARDS & IMPURITIES
EDQM
CAS Number : 171596-29-5
Quantity Per Vial : 200 mg
Sale Unit : 1
Order Code : Y0001417
Batch No : 2
Price (€) : 79
Storage : +5°C ± 3°C
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ANALYTICAL
BioAnalytical Methods
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
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PharmaCompass offers a list of Tadalafil 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 Tadalafil manufacturer or Tadalafil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tadalafil manufacturer or Tadalafil supplier.
PharmaCompass also assists you with knowing the Tadalafil API Price utilized in the formulation of products. Tadalafil API Price is not always fixed or binding as the Tadalafil Price is obtained through a variety of data sources. The Tadalafil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tadalafil Lilly manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tadalafil Lilly, including repackagers and relabelers. The FDA regulates Tadalafil Lilly manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tadalafil Lilly 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 Tadalafil Lilly manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tadalafil Lilly supplier is an individual or a company that provides Tadalafil Lilly active pharmaceutical ingredient (API) or Tadalafil Lilly finished formulations upon request. The Tadalafil Lilly suppliers may include Tadalafil Lilly API manufacturers, exporters, distributors and traders.
click here to find a list of Tadalafil Lilly suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tadalafil Lilly DMF (Drug Master File) is a document detailing the whole manufacturing process of Tadalafil Lilly active pharmaceutical ingredient (API) in detail. Different forms of Tadalafil Lilly DMFs exist exist since differing nations have different regulations, such as Tadalafil Lilly USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tadalafil Lilly DMF submitted to regulatory agencies in the US is known as a USDMF. Tadalafil Lilly USDMF includes data on Tadalafil Lilly's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tadalafil Lilly USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tadalafil Lilly suppliers with USDMF on PharmaCompass.
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 Tadalafil Lilly Drug Master File in Japan (Tadalafil Lilly JDMF) empowers Tadalafil Lilly 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 Tadalafil Lilly JDMF during the approval evaluation for pharmaceutical products. At the time of Tadalafil Lilly 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 Tadalafil Lilly suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Tadalafil Lilly Drug Master File in Korea (Tadalafil Lilly KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tadalafil Lilly. The MFDS reviews the Tadalafil Lilly KDMF as part of the drug registration process and uses the information provided in the Tadalafil Lilly KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tadalafil Lilly 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 Tadalafil Lilly API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Tadalafil Lilly suppliers with KDMF on PharmaCompass.
A Tadalafil Lilly CEP of the European Pharmacopoeia monograph is often referred to as a Tadalafil Lilly Certificate of Suitability (COS). The purpose of a Tadalafil Lilly CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tadalafil Lilly EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tadalafil Lilly to their clients by showing that a Tadalafil Lilly CEP has been issued for it. The manufacturer submits a Tadalafil Lilly CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tadalafil Lilly CEP holder for the record. Additionally, the data presented in the Tadalafil Lilly CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tadalafil Lilly DMF.
A Tadalafil Lilly CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tadalafil Lilly 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 Tadalafil Lilly suppliers with CEP (COS) on PharmaCompass.
A Tadalafil Lilly written confirmation (Tadalafil Lilly WC) is an official document issued by a regulatory agency to a Tadalafil Lilly manufacturer, verifying that the manufacturing facility of a Tadalafil Lilly active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tadalafil Lilly APIs or Tadalafil Lilly finished pharmaceutical products to another nation, regulatory agencies frequently require a Tadalafil Lilly WC (written confirmation) as part of the regulatory process.
click here to find a list of Tadalafil Lilly suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Tadalafil Lilly as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tadalafil Lilly API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Tadalafil Lilly as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Tadalafil Lilly and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tadalafil Lilly NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tadalafil Lilly suppliers with NDC on PharmaCompass.
Tadalafil Lilly 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 Tadalafil Lilly 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 Tadalafil Lilly GMP manufacturer or Tadalafil Lilly GMP API supplier for your needs.
A Tadalafil Lilly CoA (Certificate of Analysis) is a formal document that attests to Tadalafil Lilly's compliance with Tadalafil Lilly specifications and serves as a tool for batch-level quality control.
Tadalafil Lilly CoA mostly includes findings from lab analyses of a specific batch. For each Tadalafil Lilly 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.
Tadalafil Lilly may be tested according to a variety of international standards, such as European Pharmacopoeia (Tadalafil Lilly EP), Tadalafil Lilly JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tadalafil Lilly USP).
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