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Chemistry

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Also known as: 81403-68-1, Alfuzosin hcl, Uroxatral, Urion, Xatral, Alfoten
Molecular Formula
C19H28ClN5O4
Molecular Weight
425.9  g/mol
InChI Key
YTNKWDJILNVLGX-UHFFFAOYSA-N
FDA UNII
75046A1XTN

Alfuzosin HCl
Alfuzosin Hydrochloride is the hydrochloride salt of alfuzosin, a quinazoline compound with smooth muscle-relaxing activity. Alfuzosin selectively binds to and antagonizes post-synaptic alpha-1-adrenoreceptors in smooth muscle of the prostate, bladder base, bladder neck, prostatic capsule, and prostatic urethra, initiating relaxation of smooth muscle and resulting in improvement of urine flow and the symptoms of benign prostatic hyperplasia (BPH). This agent also blocks alpha-1-adrenoreceptors in peripheral vascular smooth muscle, resulting in vasodilatation and a decrease in peripheral vascular resistance.
1 2D Structure

Alfuzosin HCl

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
N-[3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)-methylamino]propyl]oxolane-2-carboxamide;hydrochloride
2.1.2 InChI
InChI=1S/C19H27N5O4.ClH/c1-24(8-5-7-21-18(25)14-6-4-9-28-14)19-22-13-11-16(27-3)15(26-2)10-12(13)17(20)23-19;/h10-11,14H,4-9H2,1-3H3,(H,21,25)(H2,20,22,23);1H
2.1.3 InChI Key
YTNKWDJILNVLGX-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CN(CCCNC(=O)C1CCCO1)C2=NC3=CC(=C(C=C3C(=N2)N)OC)OC.Cl
2.2 Other Identifiers
2.2.1 UNII
75046A1XTN
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Alfetim

2. Alfusozine

3. Alfuzosin

4. Alphuzosine

5. Benestan

6. N-(3-((4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino)propyl)tetrahydro-2-furancarboxamide

7. Urion

8. Uroxatral

9. Xatral

2.3.2 Depositor-Supplied Synonyms

1. 81403-68-1

2. Alfuzosin Hcl

3. Uroxatral

4. Urion

5. Xatral

6. Alfoten

7. Alfuzosin (hydrochloride)

8. Sl 77 499-10

9. Sl 77499-10

10. Alfuzosinhydrochloride

11. Sl-77499-10

12. 75046a1xtn

13. Alfuzosin Hydrochloride (uroxatral)

14. Alfetim

15. Sl-77-499-10

16. Dsstox_cid_25514

17. Dsstox_rid_80924

18. Dsstox_gsid_45514

19. N-(3-((4-amino-6,7-dimethoxyquinazolin-2-yl)(methyl)amino)propyl)tetrahydrofuran-2-carboxamide Hydrochloride

20. N-[3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)-methylamino]propyl]oxolane-2-carboxamide;hydrochloride

21. Sl-7749910

22. 81403-68-1 (alfuzosin Hcl), 81403-80-7(alfuzosin).

23. Alfuzosin Hydrochloride [usan]

24. Xatral Retard

25. Xatral Od

26. Xatral Sr

27. Xatral Xl

28. Chebi:32286

29. Uroxatral (tn)

30. N-[3-[(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino]propyl]tetrahydro-2-furancarboxamide, Monohydrochloride

31. Unii-75046a1xtn

32. N-(3-((4-amino-6,7-dimethoxyquinazolin-2-yl)

33. Sr-01000759345

34. Alfuzosin Hydrochloride (jan/usan)

35. Alfuzosin Hydrochloride [usan:usp]

36. Mfcd00879135

37. Sl-77499

38. Alfuzosin Hydrochloride;

39. Ncgc00016946-01

40. Sl77.0499-10

41. Cas-81403-68-1

42. Sl-77.0499-10

43. Alfuzosin Hydrochloride,(s)

44. Chembl1723

45. Alfuzosin-[d3] Hydrochloride

46. Schembl179910

47. Dtxsid3045514

48. Alfuzosin For Peak Identification

49. Hy-b0192a

50. Alfuzosin For System Suitability A

51. Bcpp000417

52. Hms1569a05

53. Alfuzosin Hydrochloride [mi]

54. Tox21_110701

55. Tox21_500224

56. Alfuzosin Hydrochloride [jan]

57. S1409

58. (methyl)amino)propyl)tetrahydrofuran-2

59. Akos015966770

60. Tox21_110701_1

61. Ac-1116

62. Alfuzosin Hydrochloride [mart.]

63. Bcp9000271

64. Ccg-213373

65. Lp00224

66. Alfuzosin Hydrochloride [usp-rs]

67. Alfuzosin Hydrochloride [who-dd]

68. Ncgc00095152-09

69. Ncgc00260909-01

70. 2-furancarboxamide, N-(3-((4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino)propyl)tetrahydro-, Monohydrochloride (+-)-

71. As-14240

72. Alfuzosin Hydrochloride [orange Book]

73. Ft-0630890

74. Sw196913-4

75. Alfuzosin Hydrochloride [ep Monograph]

76. Alfuzosin Hydrochloride [usp Monograph]

77. D01692

78. T71347

79. Alfuzosin Hydrochloride, >=98% (hplc), Solid

80. 403a681

81. A840121

82. Sr-01000759345-5

83. Q27114856

84. Alfuzosin Hydrochloride, European Pharmacopoeia (ep) Reference Standard

85. Alfuzosin Hydrochloride, United States Pharmacopeia (usp) Reference Standard

86. Alfuzosin For Peak Identification, European Pharmacopoeia (ep) Reference Standard

87. Alfuzosin For System Suitability A, European Pharmacopoeia (ep) Reference Standard

88. Alfuzosin For System Suitability, European Pharmacopoeia (ep) Reference Standard

89. Alfuzosin Hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material

90. (+/-)-n-(3-((4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino)propyl)tetrahydro-2-furamide Monohydrochloride

91. 2-furancarboxamide, (+/-)-n-(3-((4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino)propyl)tetrahydro-, Monohydrochloride

92. 4-amino-6,7-dimethoxy-2-[methyl[3-[(tetrahydro-2-furoyl)amino]propyl]amino]quinazoline Hydrochloride

93. N-(3-((4-amino-6,7-dimethoxyquinazolin-2-yl)(methyl)amino)-propyl)tetrahydrofuran-2-carboxamide Hydrochloride

94. N-[3-[(4-amino-6,7-dimethoxy-2-quinazolinyl)(methyl)amino]propyl]tetrahydro-2-furancarboxamide Hydrochloride

95. N-[3-[(4-amino-6,7-dimethoxy-2-quinazolinyl)methylamino]propyl]tetrahydro-2-furancarboxamide Hydrochloride

2.4 Create Date
2005-06-24
3 Chemical and Physical Properties
Molecular Weight 425.9 g/mol
Molecular Formula C19H28ClN5O4
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count8
Rotatable Bond Count8
Exact Mass425.1829821 g/mol
Monoisotopic Mass425.1829821 g/mol
Topological Polar Surface Area112 Ų
Heavy Atom Count29
Formal Charge0
Complexity511
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Drug Information
1 of 4  
Drug NameAlfuzosin hydrochloride
Drug LabelEach alfuzosin hydrochloride extended-release tablet contains 10 mg alfuzosin hydrochloride as the active ingredient. Alfuzosin hydrochloride is a white to off-white powder that melts at 231 to 233C. It is freely soluble in water, sparingly solub...
Active IngredientAlfuzosin hydrochloride
Dosage FormTablet, extended release
RouteOral
Strength10mg
Market StatusPrescription
CompanyWockhardt; Teva Pharms; Apotex; Aurobindo Pharma; Torrent Pharms; Invagen Pharms; Sun Pharma Global; Mylan

2 of 4  
Drug NameUroxatral
PubMed HealthAlfuzosin (By mouth)
Drug ClassesBenign Prostatic Hypertrophy Agent
Drug LabelEach UROXATRAL extended-release tablet contains 10 mg alfuzosin hydrochloride as the active ingredient. Alfuzosin hydrochloride is a white to off-white crystalline powder that melts at approximately 240C. It is freely soluble in water, sparingly so...
Active IngredientAlfuzosin hydrochloride
Dosage FormTablet, extended release
RouteOral
Strength10mg
Market StatusPrescription
CompanyCovis Pharma Sarl

3 of 4  
Drug NameAlfuzosin hydrochloride
Drug LabelEach alfuzosin hydrochloride extended-release tablet contains 10 mg alfuzosin hydrochloride as the active ingredient. Alfuzosin hydrochloride is a white to off-white powder that melts at 231 to 233C. It is freely soluble in water, sparingly solub...
Active IngredientAlfuzosin hydrochloride
Dosage FormTablet, extended release
RouteOral
Strength10mg
Market StatusPrescription
CompanyWockhardt; Teva Pharms; Apotex; Aurobindo Pharma; Torrent Pharms; Invagen Pharms; Sun Pharma Global; Mylan

4 of 4  
Drug NameUroxatral
PubMed HealthAlfuzosin (By mouth)
Drug ClassesBenign Prostatic Hypertrophy Agent
Drug LabelEach UROXATRAL extended-release tablet contains 10 mg alfuzosin hydrochloride as the active ingredient. Alfuzosin hydrochloride is a white to off-white crystalline powder that melts at approximately 240C. It is freely soluble in water, sparingly so...
Active IngredientAlfuzosin hydrochloride
Dosage FormTablet, extended release
RouteOral
Strength10mg
Market StatusPrescription
CompanyCovis Pharma Sarl

5 Pharmacology and Biochemistry
5.1 MeSH Pharmacological Classification

Urological Agents

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


Adrenergic alpha-1 Receptor Antagonists

Drugs that bind to and block the activation of ADRENERGIC ALPHA-1 RECEPTORS. (See all compounds classified as Adrenergic alpha-1 Receptor Antagonists.)


5.2 FDA Pharmacological Classification
5.2.1 Pharmacological Classes
alpha-Adrenergic Blocker [EPC]; Adrenergic alpha-Antagonists [MoA]

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V. ROAD JOGESHWARI WEST Contact No: 9198677","city":"MUMBAI","supplier":"FARMAK, A.S","supplierCountry":"CZECH REPUBLIC","foreign_port":"NA","customer":"UNICHEM LABORATORIES LIMITED","customerCountry":"INDIA","quantity":"50.00","actualQuantity":"50","unit":"KGS","unitRateFc":"1050","totalValueFC":"53393.4","currency":"USD","unitRateINR":"87832.5","date":"02-Mar-2023","totalValueINR":"4391625","totalValueInUsd":"53393.4","indian_port":"BOMBAY AIR","hs_no":"29420090","bill_no":"4875522","productDescription":"API","marketType":"REGULATED MARKET","country":"CZECH REPUBLIC","selfForZScoreResived":"Pharma Grade","supplierPort":"NA","supplierAddress":"","customerAddress":"UNICHEM BHAVAN S. V. ROAD JOGESHWARI WEST Contact No: 9198677"},{"dataSource":"API Import","activeIngredients":"","year":"2023","qtr":"Q2","strtotime":1683138600,"product":"ALFUZOSIN HYDROCHLORIDE ALFUZOSIN HYDROCHLORIDE IP","address":"UNICHEM BHAVAN S. V. ROAD,JOGESHWA RI WEST","city":"MUMBAI","supplier":"FARMAK, A.S","supplierCountry":"CZECH REPUBLIC","foreign_port":"PRAGUE RUZYNE","customer":"UNICHEM LABORATORIES LIMITED","customerCountry":"INDIA","quantity":"50.00","actualQuantity":"50","unit":"KGS","unitRateFc":"1050","totalValueFC":"53052.4","currency":"USD","unitRateINR":"87307.5","date":"04-May-2023","totalValueINR":"4365375","totalValueInUsd":"53052.4","indian_port":"BOMBAY AIR","hs_no":"29420090","bill_no":"0","productDescription":"API","marketType":"REGULATED MARKET","country":"Czech Republic","selfForZScoreResived":"Pharma Grade","supplierPort":"PRAGUE RUZYNE","supplierAddress":"","customerAddress":"UNICHEM BHAVAN S. V. ROAD,JOGESHWA RI WEST"},{"dataSource":"API Import","activeIngredients":"","year":"2024","qtr":"Q1","strtotime":1710268200,"product":"ALFUZOSIN HYDROCHLORIDE (ALFUZOSIN HYDROCHLORIDE IP)","address":"UNICHEM BHAVAN, S. V. 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ROAD"},{"dataSource":"API Import","activeIngredients":"","year":"2024","qtr":"Q2","strtotime":1714674600,"product":"ALFUZOSIN HYDROCHLORIDE IP, CAS NO. 81403-68-1, BATCH NO. 03100324, 03090324, 03080224, 03070224, 03060224, 03050224","address":"ACME PLAZA, ANDHERI KURLA ROAD,","city":"MUMBAI, MAHARASHTRA.","supplier":"FARMAK, A.S","supplierCountry":"CZECH REPUBLIC","foreign_port":"OSTRAVA","customer":"SUN PHARMACEUTICAL INDUSTRIES LIMITED","customerCountry":"INDIA","quantity":"250.00","actualQuantity":"250","unit":"KGS","unitRateFc":"950","totalValueFC":"240409.5","currency":"USD","unitRateINR":"80156.5","date":"03-May-2024","totalValueINR":"20039134.94","totalValueInUsd":"240409.5","indian_port":"Delhi Air","hs_no":"29349990","bill_no":"3309994","productDescription":"API","marketType":"REGULATED MARKET","country":"CZECH REPUBLIC","selfForZScoreResived":"Pharma Grade","supplierPort":"OSTRAVA","supplierAddress":"NA VLCINCI 16\/3 KLATERNIHRADISKO 77900 OLOMOUCSDNF CZECH REPUBLIC","customerAddress":"ACME PLAZA, ANDHERI KURLA ROAD,"},{"dataSource":"API Import","activeIngredients":"","year":"2024","qtr":"Q3","strtotime":1725301800,"product":"ALFUZOSIN HYDROCHLORIDE (ALFUZOSIN HYDROCHLORIDE IP)","address":"UNICHEM BHAVAN, S. V. ROAD","city":"MUMBAI,MAHARASHTRA.","supplier":"FARMAK, A.S","supplierCountry":"CZECH REPUBLIC","foreign_port":"PRAGUE - RUZYNE","customer":"UNICHEM LABORATORIES LIMITED","customerCountry":"INDIA","quantity":"50.00","actualQuantity":"50","unit":"KGS","unitRateFc":"1050","totalValueFC":"53157","currency":"USD","unitRateINR":"89092.5","date":"03-Sep-2024","totalValueINR":"4454625","totalValueInUsd":"53157","indian_port":"Bombay Air","hs_no":"29420090","bill_no":"5404910","productDescription":"API","marketType":"REGULATED MARKET","country":"CZECH REPUBLIC","selfForZScoreResived":"Pharma Grade","supplierPort":"PRAGUE - RUZYNE","supplierAddress":"NA VLCINCI 16\/3 KLASTERNI HRADISKO 779 0 0 OLOMOUC CZECH REPUBLIC , , Czech Republic Czech Republic Czech Republic","customerAddress":"UNICHEM BHAVAN, S. V. ROAD"}]
08-Jan-2021
16-Nov-2024
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ABOUT THIS PAGE

Alfuzosin hydrochloride; Manufacturers

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

Alfuzosin hydrochloride; Suppliers

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

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

Alfuzosin hydrochloride; USDMF

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

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

click here to find a list of Alfuzosin hydrochloride; suppliers with USDMF on PharmaCompass.

Alfuzosin hydrochloride; KDMF

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

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

After submitting a Alfuzosin hydrochloride; 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 Alfuzosin hydrochloride; API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Alfuzosin hydrochloride; suppliers with KDMF on PharmaCompass.

Alfuzosin hydrochloride; CEP

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

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

Alfuzosin hydrochloride; WC

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

click here to find a list of Alfuzosin hydrochloride; suppliers with Written Confirmation (WC) on PharmaCompass.

Alfuzosin hydrochloride; NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Alfuzosin hydrochloride; as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Alfuzosin hydrochloride; API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Alfuzosin hydrochloride; as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

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

click here to find a list of Alfuzosin hydrochloride; suppliers with NDC on PharmaCompass.

Alfuzosin hydrochloride; GMP

Alfuzosin hydrochloride; 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 Alfuzosin hydrochloride; 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 Alfuzosin hydrochloride; GMP manufacturer or Alfuzosin hydrochloride; GMP API supplier for your needs.

Alfuzosin hydrochloride; CoA

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

Alfuzosin hydrochloride; CoA mostly includes findings from lab analyses of a specific batch. For each Alfuzosin hydrochloride; 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.

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

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