Synopsis
Synopsis
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CEP/COS
0
JDMF
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VMF
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EDQM
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USP
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JP
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1. ((1r,2r,3as,9as)-2-hydroxy-1-((3s)-3-hydroxyoctyl)-2,3,3a,4,9,9a-hexahydro-1h-cylopent(b)naphthalen-5-yl)oxy)acetate
2. Orenitram
3. Remodulin
4. Trepostinil Sodium
5. Treprostinil Diethanolamine
6. Treprostinil Diolamin
7. Treprostinil Diolamine
8. Treprostinil Sodium
9. Ut-15
10. Ut-15c
1. 81846-19-7
2. Remodulin
3. Uniprost
4. Rumodolin
5. Orenitram
6. Tyvaso
7. Lrx-15
8. Ut-15
9. 15au81
10. Treprostinil Free Acid
11. Rum6k67esg
12. 2-(((1r,2r,3as,9as)-2-hydroxy-1-((s)-3-hydroxyoctyl)-2,3,3a,4,9,9a-hexahydro-1h-cyclopenta[b]naphthalen-5-yl)oxy)acetic Acid
13. Chebi:50861
14. 81846-19-7 (free Acid)
15. ((1r,2r,3as,9as)-2-hydroxy-1-((3s)-3-hydroxyoctyl)-2,3,3a,4,9,9a-hexahydro-1h-cylopent(b)naphthalen-5-yl)oxy)acetate
16. 2-[[(1r,2r,3as,9as)-2-hydroxy-1-[(3s)-3-hydroxyoctyl]-2,3,3a,4,9,9a-hexahydro-1h-cyclopenta[g]naphthalen-5-yl]oxy]acetic Acid
17. 289480-64-4
18. 15-au-81
19. L-606
20. Treprostinilo
21. Treprostinilum
22. Lrx 15
23. Treprostinil [usan:inn]
24. Remodulin (tn)
25. Unii-rum6k67esg
26. U 62840
27. Tresprostinil
28. Trevyent
29. U-62,840
30. Treprostinil [mi]
31. Treprostinil [inn]
32. Treprostinil [jan]
33. Treprostinil [usan]
34. Treprostinil [vandf]
35. Treprostinil Pound>>ut-15
36. Treprostinil [mart.]
37. Treprostinil [who-dd]
38. 15au
39. Gtpl5820
40. Schembl4349618
41. Treprostinil (jan/usan/inn)
42. Chembl1237119
43. Lrx -15
44. Dtxsid901021654
45. Hms3648g07
46. Treprostinil [orange Book]
47. Amy22230
48. Bcp10253
49. Ex-a1414
50. Zinc3800475
51. Mfcd00888847
52. Akos027470173
53. Cs-7872
54. Db00374
55. Ncgc00343944-03
56. ({(1r,2r,3as,9as)-2-hydroxy-1-[(3s)-3-hydroxyoctyl]-2,3,3a,4,9,9a-hexahydro-1h-cyclopenta[b]naphthalen-5-yl}oxy)acetic Acid
57. 2-[[(1r,2r,3as,9as)-2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-[(3s)-3-hydroxyoctyl]-1h-benz[f]inden-5-yl]oxy]acetic Acid
58. Ac-30207
59. As-56364
60. L606
61. Hy-100441
62. D06213
63. Sr-01000946210
64. Q3495231
65. Sr-01000946210-1
66. Brd-k19706299-001-01-4
67. [[(1r,2r,3as,9as)-2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-[(s)-3-hydroxyoctyl]-1h-benzo[f]indene-5-yl]oxy]acetic Acid
68. [[(1r,2r,3as,9as)-2,3,4,9,9a-hexahydro-2-hydroxy-1-[(3s)-3-hydroxyoctyl]-1h-benz[f]inden-5-yl]oxy]acetic Acid
69. 2-((1r,2r,3as,9as)-2-hydroxy-1-((s)-3-hydroxyoctyl)-2,3,3a,4,9,9a-hexahydro-1h-cyclopenta[b]naphthalen-5-yloxy)acetic Acid
70. 2-[[(1r,2r,3as,9as)-2,3,4,9,9a-hexahydro-2-hydroxy-1-[(3s)-3-hydroxyoctyl]-1h-benz[f]inden-5-yl]oxy]-acetic Acid
71. 2-[[(2r,3r,3as,9as)-2-hydroxy-3-[(3s)-3-hydroxyoctyl]-2,3,3a,4,9,9a-hexahydro-1h-cyclopenta[g]naphthalen-8-yl]oxy]acetic Acid
72. 2-{[(1r,2r,3as,9as)-2-hydroxy-1-[(3s)-3-hydroxyoctyl]-1h,2h,3h,3ah,4h,9h,9ah-cyclopenta[b]naphthalen-5-yl]oxy}acetic Acid
73. Acetic Acid, (((1r,2r,3as,9as)-2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-((3s)-3-hydroxyoctyl)-1h-benz(f)inden-5-yl)oxy)-
74. Acetic Acid, ((2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-(3-hydroxyoctyl)-1h-benz(f)inden-5-yl)oxy)-, (1r-(1alpha(s*),2beta,3aalpha,9aalpha))-
75. Acetic Acid,(((1r,2r,3as,9as)-2,3,3a,4,9,9a-hexahydro-2-hydroxy-1-((3s)-3-hydroxyoctyl)-1h-benz(f)inden-5-yl)oxy)-
| Molecular Weight | 390.5 g/mol |
|---|---|
| Molecular Formula | C23H34O5 |
| XLogP3 | 4.5 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 10 |
| Exact Mass | 390.24062418 g/mol |
| Monoisotopic Mass | 390.24062418 g/mol |
| Topological Polar Surface Area | 87 Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 495 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 1 |
| 1 of 4 | |
|---|---|
| Drug Name | Remodulin |
| PubMed Health | Treprostinil |
| Drug Classes | Antihypertensive, Cardiovascular Agent, Platelet Aggregation Inhibitor, Vasodilator |
| Drug Label | Remodulin (treprostinil) Injection is a sterile solution of treprostinil formulated for subcutaneous or intravenous administration. Remodulin is supplied in 20 mL multidose vials in four strengths, containing 20 mg, 50 mg, 100 mg, or 200 mg (1 mg/mL,... |
| Active Ingredient | Treprostinil |
| Dosage Form | Injectable |
| Route | Iv (infusion), subcutaneous |
| Strength | 1mg/ml; 2.5mg/ml; 10mg/ml; 5mg/ml |
| Market Status | Prescription |
| Company | United Therap |
| 2 of 4 | |
|---|---|
| Drug Name | Tyvaso |
| PubMed Health | Treprostinil (By breathing) |
| Drug Classes | Vasodilator |
| Drug Label | Tyvaso is a sterile formulation of treprostinil intended for administration by oral inhalation using the Tyvaso Inhalation System. Tyvaso is supplied in 2.9 mL low density polyethylene (LDPE) ampules, containing 1.74 mg treprostinil (0.6 mg/mL). Each... |
| Active Ingredient | Treprostinil |
| Dosage Form | Solution |
| Route | Inhalation |
| Strength | eq 0.6mg base/ml |
| Market Status | Prescription |
| Company | United Therap |
| 3 of 4 | |
|---|---|
| Drug Name | Remodulin |
| PubMed Health | Treprostinil |
| Drug Classes | Antihypertensive, Cardiovascular Agent, Platelet Aggregation Inhibitor, Vasodilator |
| Drug Label | Remodulin (treprostinil) Injection is a sterile solution of treprostinil formulated for subcutaneous or intravenous administration. Remodulin is supplied in 20 mL multidose vials in four strengths, containing 20 mg, 50 mg, 100 mg, or 200 mg (1 mg/mL,... |
| Active Ingredient | Treprostinil |
| Dosage Form | Injectable |
| Route | Iv (infusion), subcutaneous |
| Strength | 1mg/ml; 2.5mg/ml; 10mg/ml; 5mg/ml |
| Market Status | Prescription |
| Company | United Therap |
| 4 of 4 | |
|---|---|
| Drug Name | Tyvaso |
| PubMed Health | Treprostinil (By breathing) |
| Drug Classes | Vasodilator |
| Drug Label | Tyvaso is a sterile formulation of treprostinil intended for administration by oral inhalation using the Tyvaso Inhalation System. Tyvaso is supplied in 2.9 mL low density polyethylene (LDPE) ampules, containing 1.74 mg treprostinil (0.6 mg/mL). Each... |
| Active Ingredient | Treprostinil |
| Dosage Form | Solution |
| Route | Inhalation |
| Strength | eq 0.6mg base/ml |
| Market Status | Prescription |
| Company | United Therap |
For use as a continuous subcutaneous infusion or intravenous infusion (for those not able to tolerate a subcutaneous infusion) for the treatment of pulmonary arterial hypertension in patients with NYHA Class II-IV symptoms to diminish symptoms associated with exercise.
FDA Label
Treatment of adult patients with WHO Functional Class (FC) III or IV and:
- inoperable chronic thromboembolic pulmonary hypertension (CTEPH), or
- persistent or recurrent CTEPH after surgical treatment
to improve exercise capacity.
Treatment of pulmonary arterial hypertension
Pulmonary arterial hypertension (PAH) is a disease in which blood pressure is abnormally high in the arteries between the heart and lungs. PAH is characterized by symptoms of shortness of breath during physical exertion. The condition can ultimately lead to heart failure. Treprostinil is a potent oral antiplatelet agent. The major pharmacologic actions of treprostinil are direct vasodilation of pulmonary and systemic arterial vascular beds and inhibition of platelet aggregation. In animals, the vasodilatory effects reduce right and left ventricular afterload and increase cardiac output and stroke volume. Other studies have shown that treprostinil causes a dose-related negative inotropic and lusitropic effect. No major effects on cardiac conduction have been observed.
Antihypertensive Agents
Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. (See all compounds classified as Antihypertensive Agents.)
B01AC21
B - Blood and blood forming organs
B01 - Antithrombotic agents
B01A - Antithrombotic agents
B01AC - Platelet aggregation inhibitors excl. heparin
B01AC21 - Treprostinil
Absorption
Relatively rapid and complete after subcutaneous infusion, with an absolute bioavailability approximately 100%. In patients with mild (n=4) or moderate (n=5) hepatic insufficiency and portopulmonary hypertension following a subcutaneous dose of 10 ng per kg of body weight per min for 150 mins the AUC 0-∞ was increased 3-fold and 5-fold respectively.
Volume of Distribution
14 L/70 kg
Substantially metabolized by the liver, but the precise enzymes responsible are unknown. Five metabolites have been described (HU1 through HU5) however, the biological activity and metabolic fate of these are unknown. The chemical structure of HU1 is unknown. The metabolite HU5 is the glucuronide conjugate of treprostinil. The other metabolites are formed by oxidation of the 3-hydroxyoctyl side chain (HU2) and subsequent additional oxidation (HU3) or dehydration (HU4). Study results of in vitro human hepatic cytochrome P450 demonstrates that treprostinil does not inhibit CYP-1A2, 2C9, 2C19, 2D6, 2E1, or 3A. There have been no studies that evaluate the potential of treprostinil to induce these enzymes.
Terminal elimination half-life is approximately 2 to 4 hours. Plasma half-life is 34 and 85 minutes for intravenous and subcutaneous infusion of the drug, respectively.
The major pharmacological actions of treprostinil are direct vasodilation of pulmonary and systemic arterial vascular beds and inhibition of platelet aggregation. In addition to treprostinil's direct vasodilatory effects, it also inhibits inflammatory cytokine. As a synthetic analogue of prostacyclin, it binds to the prostacyclin receptor, which subsequently induces the aforementioned downstream effects.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28340
Submission : 2016-08-15
Status : Active
Type : II
NDC Package Code : 68245-0008
Start Marketing Date : 2010-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-02-16
Pay. Date : 2016-09-20
DMF Number : 30861
Submission : 2016-09-27
Status : Active
Type : II
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm :
NDC Package Code : 58159-041
Start Marketing Date : 2016-07-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-05-23
Pay. Date : 2016-11-25
DMF Number : 31145
Submission : 2016-12-09
Status : Active
Type : II
NDC Package Code : 82231-115
Start Marketing Date : 2019-11-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-01-06
Pay. Date : 2014-07-15
DMF Number : 28458
Submission : 2014-09-16
Status : Active
Type : II
NDC Package Code : 68245-0009
Start Marketing Date : 2010-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29207
Submission : 2015-08-12
Status : Active
Type : II
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-040
Start Marketing Date : 2016-06-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
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API Imports and Exports
| Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
|---|
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Details:
Treprostinil are direct vasodilation of pulmonary and systemic arterial vascular beds, and inhibition of platelet aggregation. It is indicated for the treatment for pulmonary arterial hypertension.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Cardiology/Vascular Diseases Brand Name: Remodulin-Generic
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable April 21, 2023
Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Cardiology/Vascular Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Dr. Reddy's Laboratories Announces the Launch of Treprostinil Injection in the U.S.
Details : Treprostinil are direct vasodilation of pulmonary and systemic arterial vascular beds, and inhibition of platelet aggregation. It is indicated for the treatment for pulmonary arterial hypertension.
Product Name : Remodulin-Generic
Product Type : Miscellaneous
Upfront Cash : Inapplicable
April 21, 2023
Details:
Treprostinil is a solution for infusion and act as platelet aggregation, which being evaluated for the treatment of patients with pulmonary arterial hypertension.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Cardiology/Vascular Diseases Brand Name: Remodulin-Generic
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable March 12, 2022
Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Cardiology/Vascular Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Dr. Reddy's Gets CDSCO Panel Nod to Manufacture & Market Treprostinil Solution for Infusion
Details : Treprostinil is a solution for infusion and act as platelet aggregation, which being evaluated for the treatment of patients with pulmonary arterial hypertension.
Product Name : Remodulin-Generic
Product Type : Miscellaneous
Upfront Cash : Inapplicable
March 12, 2022
Details:
Treprostinil is a Other Small Molecule drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of Hypertension, Pulmonary.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Pulmonary/Respiratory Diseases Brand Name: Undisclosed
Study Phase: Phase IProduct Type: Miscellaneous
Sponsor: United Therapeutics
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 11, 2025

Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Pulmonary/Respiratory Diseases
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : United Therapeutics
Deal Size : Inapplicable
Deal Type : Inapplicable
Inhaled Treprostinil Effect on Exercise in Pulmonary Hypertension
Details : Treprostinil is a Other Small Molecule drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of Hypertension, Pulmonary.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
August 11, 2025

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Details:
Treprostinil is a Other Small Molecule drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of Pulmonary Disease, Chronic Obstructive.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Pulmonary/Respiratory Diseases Brand Name: Undisclosed
Study Phase: Phase IProduct Type: Miscellaneous
Sponsor: Yuh Chin T Huang, MD, MHS
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable June 26, 2025

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Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Pulmonary/Respiratory Diseases
Highest Development Status : Phase I
Partner/Sponsor/Collaborator : Yuh Chin T Huang, MD, MHS
Deal Size : Inapplicable
Deal Type : Inapplicable
Inhaled Treprostinil (Tyvaso Nebulizer) For COPD Patients with Hypoxemia
Details : Treprostinil is a Other Small Molecule drug candidate, which is currently being evaluated in Phase I clinical studies for the treatment of Pulmonary Disease, Chronic Obstructive.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
June 26, 2025

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Details:
The financing for Treprostinil Sodium will support research targeting the Prostanoid IP receptor in pulmonary arterial hypertension.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Cardiology/Vascular Diseases Brand Name: Yutrepia
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Healthcare Royalty
Deal Size: $50.0 million Upfront Cash: Undisclosed
Deal Type: Financing June 23, 2025

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Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Cardiology/Vascular Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Healthcare Royalty
Deal Size : $50.0 million
Deal Type : Financing
Liquidia Gets $50M from HCRx After First YUTREPIA™ Sale
Details : The financing for Treprostinil Sodium will support research targeting the Prostanoid IP receptor in pulmonary arterial hypertension.
Product Name : Yutrepia
Product Type : Miscellaneous
Upfront Cash : Undisclosed
June 23, 2025

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Details:
Yutrepia is an FDA-approved, inhaled dry-powder formulation of treprostinil indicated for the treatment of pulmonary hypertension.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Cardiology/Vascular Diseases Brand Name: Yutrepia
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable May 23, 2025

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Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Cardiology/Vascular Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
FDA Okays Liquidia’s YUTREPIA Inhalation for PAH and PH-ILD Patients
Details : Yutrepia is an FDA-approved, inhaled dry-powder formulation of treprostinil indicated for the treatment of pulmonary hypertension.
Product Name : Yutrepia
Product Type : Miscellaneous
Upfront Cash : Inapplicable
May 23, 2025

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Details:
TRX-248 transdermal system, a once-daily transdermal patch delivering treprostinil, a prostaglandin mimetic, for the treatment of Pulmonary Arterial Hypertension (PAH).
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Cardiology/Vascular Diseases Brand Name: Undisclosed
Study Phase: PreclinicalProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable March 17, 2025

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Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Cardiology/Vascular Diseases
Highest Development Status : Preclinical
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Corsair Completes Preclinical Program for Treprostinil Prodrug Patch
Details : TRX-248 transdermal system, a once-daily transdermal patch delivering treprostinil, a prostaglandin mimetic, for the treatment of Pulmonary Arterial Hypertension (PAH).
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : Inapplicable
March 17, 2025

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Details:
Tyvaso (treprostinil sodium) inhalation solution is an approved prostaglandin agonist. It is under investigation for the treatment of pulmonary arterial hypertension.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Pulmonary/Respiratory Diseases Brand Name: Tyvaso
Study Phase: Phase IIIProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable February 04, 2025

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Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Pulmonary/Respiratory Diseases
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
United Therapeutics Completes Enrollment for TETON 1 Inhaled Treprostinil in IPF
Details : Tyvaso (treprostinil sodium) inhalation solution is an approved prostaglandin agonist. It is under investigation for the treatment of pulmonary arterial hypertension.
Product Name : Tyvaso
Product Type : Miscellaneous
Upfront Cash : Inapplicable
February 04, 2025

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Details:
The agreement aims for the development and commercialization of L606, an inhaled, sustained-release formulation of treprostinil being evaluated for the treatment of PAH and PH-ILD.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Cardiology/Vascular Diseases Brand Name: Undisclosed
Study Phase: Phase IIIProduct Type: Miscellaneous
Sponsor: Liquidia Corporation
Deal Size: $161.2 million Upfront Cash: $3.5 million
Deal Type: Expanded Collaboration October 04, 2024

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Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Cardiology/Vascular Diseases
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Liquidia Corporation
Deal Size : $161.2 million
Deal Type : Expanded Collaboration
Pharmosa Biopharm Expands Liquida Collaboration for Smart Nebulizers
Details : The agreement aims for the development and commercialization of L606, an inhaled, sustained-release formulation of treprostinil being evaluated for the treatment of PAH and PH-ILD.
Product Name : Undisclosed
Product Type : Miscellaneous
Upfront Cash : $3.5 million
October 04, 2024

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Details:
Tyvaso (treprostinil sodium) inhalation solution is an approved prostaglandin agonist. It is under investigation for the treatment of pulmonary arterial hypertension.
Lead Product(s): Treprostinil Sodium,Inapplicable
Therapeutic Area: Pulmonary/Respiratory Diseases Brand Name: Tyvaso
Study Phase: Phase IIIProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable July 10, 2024

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Lead Product(s) : Treprostinil Sodium,Inapplicable
Therapeutic Area : Pulmonary/Respiratory Diseases
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
United Therapeutics Completes Enrollment of TETON 2 Study for Inhaled Treprostinil
Details : Tyvaso (treprostinil sodium) inhalation solution is an approved prostaglandin agonist. It is under investigation for the treatment of pulmonary arterial hypertension.
Product Name : Tyvaso
Product Type : Miscellaneous
Upfront Cash : Inapplicable
July 10, 2024

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PharmaCompass offers a list of Treprostinil Sodium 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 Treprostinil Sodium manufacturer or Treprostinil Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Treprostinil Sodium manufacturer or Treprostinil Sodium supplier.
PharmaCompass also assists you with knowing the Treprostinil Sodium API Price utilized in the formulation of products. Treprostinil Sodium API Price is not always fixed or binding as the Treprostinil Sodium Price is obtained through a variety of data sources. The Treprostinil Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Treprostinil Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Treprostinil Sodium, including repackagers and relabelers. The FDA regulates Treprostinil Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Treprostinil Sodium 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 Treprostinil Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Treprostinil Sodium supplier is an individual or a company that provides Treprostinil Sodium active pharmaceutical ingredient (API) or Treprostinil Sodium finished formulations upon request. The Treprostinil Sodium suppliers may include Treprostinil Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Treprostinil Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Treprostinil Sodium DMF (Drug Master File) is a document detailing the whole manufacturing process of Treprostinil Sodium active pharmaceutical ingredient (API) in detail. Different forms of Treprostinil Sodium DMFs exist exist since differing nations have different regulations, such as Treprostinil Sodium USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Treprostinil Sodium DMF submitted to regulatory agencies in the US is known as a USDMF. Treprostinil Sodium USDMF includes data on Treprostinil Sodium's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Treprostinil Sodium USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Treprostinil Sodium suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Treprostinil Sodium Drug Master File in Korea (Treprostinil Sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Treprostinil Sodium. The MFDS reviews the Treprostinil Sodium KDMF as part of the drug registration process and uses the information provided in the Treprostinil Sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Treprostinil Sodium 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 Treprostinil Sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Treprostinil Sodium suppliers with KDMF on PharmaCompass.
A Treprostinil Sodium written confirmation (Treprostinil Sodium WC) is an official document issued by a regulatory agency to a Treprostinil Sodium manufacturer, verifying that the manufacturing facility of a Treprostinil Sodium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Treprostinil Sodium APIs or Treprostinil Sodium finished pharmaceutical products to another nation, regulatory agencies frequently require a Treprostinil Sodium WC (written confirmation) as part of the regulatory process.
click here to find a list of Treprostinil Sodium 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 Treprostinil Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Treprostinil Sodium 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 Treprostinil Sodium 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 Treprostinil Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Treprostinil Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Treprostinil Sodium suppliers with NDC on PharmaCompass.
Treprostinil Sodium 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 Treprostinil Sodium 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 Treprostinil Sodium GMP manufacturer or Treprostinil Sodium GMP API supplier for your needs.
A Treprostinil Sodium CoA (Certificate of Analysis) is a formal document that attests to Treprostinil Sodium's compliance with Treprostinil Sodium specifications and serves as a tool for batch-level quality control.
Treprostinil Sodium CoA mostly includes findings from lab analyses of a specific batch. For each Treprostinil Sodium 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.
Treprostinil Sodium may be tested according to a variety of international standards, such as European Pharmacopoeia (Treprostinil Sodium EP), Treprostinil Sodium JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Treprostinil Sodium USP).