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1. Benazapril
2. Benazepril
3. Benzazepril
4. Briem
5. Cgs-14824-a
6. Cgs-14824a
7. Cibacne
8. Cibacen
9. Labopal
10. Lotensin
1. 86541-74-4
2. Benazepril Hcl
3. Lotensin
4. Cibacen
5. Cibacene
6. Briem
7. Tensanil
8. Zinadril
9. Cibace
10. Labopol
11. Cgs 14824a Hcl
12. Benazepril (hydrochloride)
13. Cgs 14824a
14. Nsc-758920
15. Cgs-14824a Hcl
16. Chebi:3012
17. N1sn99t69t
18. (3s)-3-(((1s)-1-carboxy-3-phenylpropyl)amino)-2,3,4,5-tetrahydro-2-oxo-1h-1-benzazepine-1-acetic Acid, 3-ethyl Ester, Monohydrochloride
19. (3s)-3-[[(1s)-1-(ethoxycarbonyl)-3-phenylpropyl]amino]-2,3,4,5-tetrahydro-2-oxo-1h-1-benzazepine-1-acetic Acid Hydrochloride
20. 86541-74-4 (hcl)
21. Cibacen Chf
22. Dsstox_cid_25922
23. Dsstox_rid_81225
24. Dsstox_gsid_45922
25. 1h-1-benzazepine-1-acetic Acid, 3-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-2,3,4,5-tetrahydro-2-oxo-, Monohydrochloride, (s-(r*,r*))-
26. 2-((s)-3-(((s)-1-ethoxy-1-oxo-4-phenylbutan-2-yl)amino)-2-oxo-2,3,4,5-tetrahydro-1h-benzo[b]azepin-1-yl)acetic Acid Hydrochloride
27. 2-[(3s)-3-[[(2s)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]-2-oxo-4,5-dihydro-3h-1-benzazepin-1-yl]acetic Acid;hydrochloride
28. 2-[(3s)-3-{[(2s)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino}-2-oxo-2,3,4,5-tetrahydro-1h-1-benzazepin-1-yl]acetic Acid Hydrochloride
29. Smr000469199
30. Cas-86541-74-4
31. Mfcd00895734
32. Unii-n1sn99t69t
33. Ncgc00095132-01
34. Lotensin (tn)
35. 2-((s)-3-((s)-1-ethoxy-1-oxo-4-phenylbutan-2-ylamino)-2-oxo-2,3,4,5-tetrahydro-1h-benzo[b]azepin-1-yl)acetic Acid Hydrochloride
36. Benazeprilhydrochloride
37. Benazepril Hydrochloride [usan:usp:jan]
38. Benazepril Monohydrochloride
39. Chembl1694
40. Schembl42194
41. Benazepril Hydrochloride,(s)
42. Mls001076668
43. Mls001333171
44. Mls001333172
45. Mls001401429
46. Spectrum1505200
47. Benazepril Hydrochloride- Bio-x
48. Dtxsid9045922
49. Benazepril For System Suitability
50. Hy-b0093a
51. Bcpp000350
52. Hms1922l07
53. Pharmakon1600-01505200
54. Twt-8154
55. Benazepril Hydrochloride (jan/usp)
56. Tox21_111441
57. Benazepril Hydrochloride [mi]
58. Ccg-39520
59. Nsc758920
60. S1284
61. Benazepril Hydrochloride [jan]
62. Akos015888536
63. Tox21_111441_1
64. Bcp9000387
65. Benazepril Hydrochloride [hsdb]
66. Benazepril Hydrochloride [usan]
67. Cs-1796
68. Ks-1397
69. Nc00211
70. Nsc 758920
71. Benazepril Hydrochloride [mart.]
72. Benazepril Hydrochloride [usp-rs]
73. Benazepril Hydrochloride [who-dd]
74. Ncgc00165740-05
75. (3s)-3-[(1s)-1-ethoxycarbonyl-3-phenylpropyl]amino-2,3,4,5-tetrahydro-2-oxo-1h-1-benzazepine-1-acetic Acid Hydrochloride
76. 1h-1-benzazepine-1-acetic Acid, 2,3,4,5-tetrahydro-3-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-2-oxo-, Monohydrochloride, (s-(r*,r*))-
77. Bb164237
78. B3611
79. Sw197591-3
80. Benazepril Hydrochloride [ep Impurity]
81. Benazepril Hydrochloride [orange Book]
82. Benazepril Hydrochloride [usp Impurity]
83. Benazepril Hydrochloride [usp Monograph]
84. C07701
85. D00620
86. Lotrel Component Benazepril Hydrochloride
87. Benazepril Hydrochloride, >=98% (hplc), Solid
88. A841712
89. Benazepril Hydrochloride Component Cardalis
90. Benazepril Hydrochloride Component Of Lotrel
91. Cardalis Component Benazepril Hydrochloride
92. Sr-01000762893
93. Sr-01000762893-3
94. Benazepril Hydrochloride [ema Epar Veterinary]
95. Fortekor Plus Component Benazepril Hydrochloride
96. Lotensin Hct Component Benazepril Hydrochloride
97. Q27105927
98. Benazepril Hydrochloride Component Of Lotensin Hct
99. Benazepril Hydrochloride Component Of Fortekor Plus
100. Benazepril Hydrochloride, Vetranal(tm), Analytical Standard
101. Benazepril Hydrochloride, European Pharmacopoeia (ep) Reference Standard
102. Benazepril For System Suitability, European Pharmacopoeia (ep) Reference Standard
103. Benazepril Hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
104. Benazepril Hydrochloride, United States Pharmacopeia (usp) Reference Standard
105. [(3s)-3-{[(2s)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino}-2-oxo-2,3,4,5-tetrahydro-1h-1-benzazepin-1-yl]acetic Acid Hydrochloride
106. 2-[(3s)-3-[[(1s)-1-ethoxycarbonyl-3-phenyl-propyl]amino]-2-oxo-4,5-dihydro-3h-1-benzazepin-1-yl]acetic Acid Hydrochloride;benazepril Hydrochloride
Molecular Weight | 460.9 g/mol |
---|---|
Molecular Formula | C24H29ClN2O5 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 6 |
Rotatable Bond Count | 10 |
Exact Mass | 460.1764997 g/mol |
Monoisotopic Mass | 460.1764997 g/mol |
Topological Polar Surface Area | 95.9 Ų |
Heavy Atom Count | 32 |
Formal Charge | 0 |
Complexity | 619 |
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 | 2 |
1 of 4 | |
---|---|
Drug Name | Benazepril hydrochloride |
PubMed Health | Benazepril (By mouth) |
Drug Classes | Antihypertensive, Cardiovascular Agent, Renal Protective Agent |
Drug Label | Benazepril hydrochloride is a white to off-white crystalline powder, soluble (> 100 mg/mL) in water, in ethanol, and in methanol. BenazeprilC24H28N2O5HCl M.W. 460.96Benazeprilat, the active metabolite of benazepril, is a non-sulfhydryl angiotensin-co.. |
Active Ingredient | Benazepril hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 5mg; 10mg; 40mg; 20mg |
Market Status | Prescription |
Company | Ranbaxy; Ivax Sub Teva Pharms; Actavis Labs Fl; Teva; Apotex; Aurobindo Pharma; Zydus Pharms Usa; Biokey; Sandoz; Prinston; Mylan |
2 of 4 | |
---|---|
Drug Name | Lotensin |
Drug Label | Benazepril hydrochloride is a white to off-white crystalline powder, soluble (>100 mg/mL) in water, in ethanol, and in methanol. Its chemical name is benazepril 3-[[1-(ethoxy-carbonyl)-3-phenyl-(1S)-propyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-(3S)-be.. |
Active Ingredient | Benazepril hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 5mg; 10mg; 40mg; 20mg |
Market Status | Prescription |
Company | Us Pharms Holdings I |
3 of 4 | |
---|---|
Drug Name | Benazepril hydrochloride |
PubMed Health | Benazepril (By mouth) |
Drug Classes | Antihypertensive, Cardiovascular Agent, Renal Protective Agent |
Drug Label | Benazepril hydrochloride is a white to off-white crystalline powder, soluble (> 100 mg/mL) in water, in ethanol, and in methanol. BenazeprilC24H28N2O5HCl M.W. 460.96Benazeprilat, the active metabolite of benazepril, is a non-sulfhydryl angiotensin-co.. |
Active Ingredient | Benazepril hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 5mg; 10mg; 40mg; 20mg |
Market Status | Prescription |
Company | Ranbaxy; Ivax Sub Teva Pharms; Actavis Labs Fl; Teva; Apotex; Aurobindo Pharma; Zydus Pharms Usa; Biokey; Sandoz; Prinston; Mylan |
4 of 4 | |
---|---|
Drug Name | Lotensin |
Drug Label | Benazepril hydrochloride is a white to off-white crystalline powder, soluble (>100 mg/mL) in water, in ethanol, and in methanol. Its chemical name is benazepril 3-[[1-(ethoxy-carbonyl)-3-phenyl-(1S)-propyl]amino]-2,3,4,5-tetrahydro-2-oxo-1H-1-(3S)-be.. |
Active Ingredient | Benazepril hydrochloride |
Dosage Form | Tablet |
Route | Oral |
Strength | 5mg; 10mg; 40mg; 20mg |
Market Status | Prescription |
Company | Us Pharms Holdings I |
Angiotensin-Converting Enzyme Inhibitors
A class of drugs whose main indications are the treatment of hypertension and heart failure. They exert their hemodynamic effect mainly by inhibiting the renin-angiotensin system. They also modulate sympathetic nervous system activity and increase prostaglandin synthesis. They cause mainly vasodilation and mild natriuresis without affecting heart rate and contractility. (See all compounds classified as Angiotensin-Converting Enzyme Inhibitors.)
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.)
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Importing Country | Total Quantity (KGS) |
Average Price (USD/KGS) |
Number of Transactions |
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ABOUT THIS PAGE
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PharmaCompass offers a list of Benazepril Hydrochloride 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 Benazepril Hydrochloride manufacturer or Benazepril Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benazepril Hydrochloride manufacturer or Benazepril Hydrochloride supplier.
PharmaCompass also assists you with knowing the Benazepril Hydrochloride API Price utilized in the formulation of products. Benazepril Hydrochloride API Price is not always fixed or binding as the Benazepril Hydrochloride Price is obtained through a variety of data sources. The Benazepril Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zinadril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zinadril, including repackagers and relabelers. The FDA regulates Zinadril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zinadril 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 Zinadril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zinadril supplier is an individual or a company that provides Zinadril active pharmaceutical ingredient (API) or Zinadril finished formulations upon request. The Zinadril suppliers may include Zinadril API manufacturers, exporters, distributors and traders.
click here to find a list of Zinadril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zinadril DMF (Drug Master File) is a document detailing the whole manufacturing process of Zinadril active pharmaceutical ingredient (API) in detail. Different forms of Zinadril DMFs exist exist since differing nations have different regulations, such as Zinadril USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zinadril DMF submitted to regulatory agencies in the US is known as a USDMF. Zinadril USDMF includes data on Zinadril's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zinadril USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zinadril 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 Zinadril Drug Master File in Japan (Zinadril JDMF) empowers Zinadril 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 Zinadril JDMF during the approval evaluation for pharmaceutical products. At the time of Zinadril 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 Zinadril suppliers with JDMF on PharmaCompass.
A Zinadril CEP of the European Pharmacopoeia monograph is often referred to as a Zinadril Certificate of Suitability (COS). The purpose of a Zinadril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zinadril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zinadril to their clients by showing that a Zinadril CEP has been issued for it. The manufacturer submits a Zinadril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zinadril CEP holder for the record. Additionally, the data presented in the Zinadril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zinadril DMF.
A Zinadril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zinadril 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 Zinadril suppliers with CEP (COS) on PharmaCompass.
A Zinadril written confirmation (Zinadril WC) is an official document issued by a regulatory agency to a Zinadril manufacturer, verifying that the manufacturing facility of a Zinadril active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zinadril APIs or Zinadril finished pharmaceutical products to another nation, regulatory agencies frequently require a Zinadril WC (written confirmation) as part of the regulatory process.
click here to find a list of Zinadril 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 Zinadril as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zinadril 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 Zinadril 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 Zinadril and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zinadril NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zinadril suppliers with NDC on PharmaCompass.
Zinadril 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 Zinadril 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 Zinadril GMP manufacturer or Zinadril GMP API supplier for your needs.
A Zinadril CoA (Certificate of Analysis) is a formal document that attests to Zinadril's compliance with Zinadril specifications and serves as a tool for batch-level quality control.
Zinadril CoA mostly includes findings from lab analyses of a specific batch. For each Zinadril 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.
Zinadril may be tested according to a variety of international standards, such as European Pharmacopoeia (Zinadril EP), Zinadril JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zinadril USP).