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    Chemistry

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    Also known as: Rifaxidin, Rifacol, 80621-81-4, Rifamycin l 105, Xifaxan, Rifamycin l 105sv
    Molecular Formula
    C43H51N3O11
    Molecular Weight
    785.9  g/mol
    InChI Key
    NZCRJKRKKOLAOJ-XRCRFVBUSA-N
    FDA UNII
    L36O5T016N
    Rifaximin
    A synthetic rifamycin derivative and anti-bacterial agent that is used for the treatment of GASTROENTERITIS caused by ESCHERICHIA COLI INFECTIONS. It may also be used in the treatment of HEPATIC ENCEPHALOPATHY.
    Rifaximin is a Rifamycin Antibacterial.
    1 2D Structure

    Rifaximin

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    [(7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z)-2,15,17,36-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22,30-octamethyl-6,23-dioxo-8,37-dioxa-24,27,33-triazahexacyclo[23.10.1.14,7.05,35.026,34.027,32]heptatriaconta-1(35),2,4,9,19,21,25(36),26(34),28,30,32-undecaen-13-yl] acetate
    2.1.2 InChI
    InChI=1S/C43H51N3O11/c1-19-14-16-46-28(18-19)44-32-29-30-37(50)25(7)40-31(29)41(52)43(9,57-40)55-17-15-27(54-10)22(4)39(56-26(8)47)24(6)36(49)23(5)35(48)20(2)12-11-13-21(3)42(53)45-33(34(32)46)38(30)51/h11-18,20,22-24,27,35-36,39,48-51H,1-10H3,(H,45,53)/b12-11+,17-15+,21-13-/t20-,22+,23+,24+,27-,35-,36+,39+,43-/m0/s1
    2.1.3 InChI Key
    NZCRJKRKKOLAOJ-XRCRFVBUSA-N
    2.1.4 Canonical SMILES
    CC1C=CC=C(C(=O)NC2=C(C3=C(C4=C(C(=C3O)C)OC(C4=O)(OC=CC(C(C(C(C(C(C1O)C)O)C)OC(=O)C)C)OC)C)C5=C2N6C=CC(=CC6=N5)C)O)C
    2.1.5 Isomeric SMILES
    C[C@H]1/C=C/C=C(\C(=O)NC2=C(C3=C(C4=C(C(=C3O)C)O[C@@](C4=O)(O/C=C/[C@@H]([C@H]([C@H]([C@@H]([C@@H]([C@@H]([C@H]1O)C)O)C)OC(=O)C)C)OC)C)C5=C2N6C=CC(=CC6=N5)C)O)/C
    2.2 Other Identifiers
    2.2.1 UNII
    L36O5T016N
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 4-deoxy-4'-methylpyrido(1',2'-1,2)imidazo(5,4c)rifamycin

    2. L 105

    3. L-105

    4. L105

    5. Redactiv

    6. Xifaxan

    2.3.2 Depositor-Supplied Synonyms

    1. Rifaxidin

    2. Rifacol

    3. 80621-81-4

    4. Rifamycin L 105

    5. Xifaxan

    6. Rifamycin L 105sv

    7. Fatroximin

    8. Rifaximine

    9. Normix

    10. Rifaximina

    11. Xifaxsan

    12. L-105

    13. Rifamixin

    14. Rifaximine [french]

    15. Rifaximinum [latin]

    16. Rifaximina [spanish]

    17. Ritacol

    18. Chebi:75246

    19. 4-deoxy-4'-methylpyrido(1',2'-1,2)imidazo(5,4-c)rifamycin Sv

    20. L36o5t016n

    21. Rifaximin (xifaxan)

    22. Nsc-758957

    23. Rifaximinum

    24. Brn 3584528

    25. (2s,16z,18e,20s,21s,22r,23r,24r,25s,26r,27s,28e)-5,6,21,23-tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-1,15-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)furo[2'',3'':7',8']naphtho[1',2':4,5]imidazo[1,2-a]pyridin-25-yl Acetate

    26. C43h51n3o11

    27. Rifaxin

    28. Redactiv

    29. Ido[1,2-a]benzimidazol-25-yl Acetate

    30. (2s,16z,18e,20s,21s,22r,23r,24r,25s,26r,27s,28e)-25-(acetyloxy)-5,6,21,23-tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-2,7-(epoxypentadeca[1,11,13]trienimino)benzofuro[4,5-e]pyrido[1,2-a]benzimidazole-1,15(2h)-dione

    31. L 105sv

    32. L 105 (ansamacrolide Antibiotic)

    33. L 105

    34. Rifaximinun

    35. Flonorm

    36. Lumenax

    37. Spiraxin

    38. Lormyx

    39. Rifaximin [usan:inn:ban]

    40. Unii-l36o5t016n

    41. 5-yl Acetate

    42. Ncgc00095842-01

    43. (2s,16z,18e,20s,21s,22r,23r,24r,25s,26r,27s,28e)-25-(acetyloxy)-5,6,21,23-tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-2,7-(epoxypentadeca(1,11,13)trienimino)benzofuro(4,5-e)pyrido(1,2-a)benzimidazole-1,15(2h)-dione

    44. (2s,16z,18e,20s,21s,22r,23r,24r,25s,26r,27s,28e)5,6,21,23-tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-1,15-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)[1]benzofuro[4,5-e]pyr

    45. Xifaxan (tn)

    46. Mfcd00864973

    47. Rifaximin [inn]

    48. Rifaximin [jan]

    49. Rifaximin [mi]

    50. Rifaximin [usan]

    51. Rifaximin [vandf]

    52. Rifaximin [mart.]

    53. Alpha-0817185

    54. Rifaximin [who-dd]

    55. Chembl1617

    56. Dsstox_cid_25998

    57. Dsstox_rid_81280

    58. Dsstox_gsid_45998

    59. (2s,16z,18e,20s,21s,22r,23r,24r,25s,26s,27s,28e)-5,6,21,23,25 Pentahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-2,7-(epoxypentadeca(1,11,13)trienimino)benzofuro(4,5-e)pyrido(1,2-a)benzimidazole-1,15(2h)-dione, 25-acetate

    60. Rifaximin (jan/usan/inn)

    61. Schembl124066

    62. Rifaximin [ep Impurity]

    63. Rifaximin [orange Book]

    64. Dtxsid7045998

    65. Rifaximin [ep Monograph]

    66. Gtpl12012

    67. Hms3715b19

    68. 88747-56-2

    69. Tox21_111529

    70. Bdbm50347620

    71. S1790

    72. Akos015963053

    73. Zinc169621200

    74. Ccg-221129

    75. Db01220

    76. Nsc 758957

    77. Rifaximin 100 Microg/ml In Acetonitrile

    78. 2,7-(epoxy(1,11,13)pentadecatrienoimino)furo(2'',3'':7',8')naphth(1',2':4,5)imidazo(1,2-a)pyridine-1,15(2h)-dione, 25-(acetyloxy)-5,6,21,23-tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-, ( 2s,16z,18e,20s,21s,22r,23r,24r,25s,26r,27s,28e)-

    79. 2,7-(epoxypentadeca(1,11,13)trienimino)benzofuro(4,5-e)pyrido(1,2-a)benzimidazole-1,15(2h)-dione, 25-(acetyloxy)-5,6,21,23-tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-, (2s-(2r*,16z,18e,20r*,21r*,22s*,23s*,24s*,25r*,26s*,27r*,28e))-

    80. Ac-19112

    81. Cas-80621-81-4

    82. L/105

    83. D02554

    84. Ab01209738-01

    85. Ab01209738-03

    86. Ab01209738_04

    87. Rifaximin, Antibiotic For Culture Media Use Only

    88. 621r814

    89. Q416073

    90. Q-201671

    91. (2s,16z,18e,20s,21s,22r,23r,24r,25s,26r,27s,28e)-5,6,21,23-tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-1,1

    92. (7s,11s,12r,13s,14r,15r,16r,17s,18s)-2,15,17,36-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22,30-octamethyl-6,23-dioxo-8,37-dioxa-24,27,33-triazahexacyclo[23.10.1.1^{4,7}.0^{5,35}.0^{26,34}.0^{27,32}]heptatriaconta-1,3,5(35),9,19,21,25(36),26(34),28,30,32-undecaen-13-yl Acetate

    93. [(7s,9e,11s,12r,13s,14r,15r,16r,17s,18s,19e,21z)-2,15,17,36-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22,30-octamethyl-6,23-dioxo-8,37-dioxa-24,27,33-triazahexacyclo[23.10.1.14,7.05,35.026,34.027,32]heptatriaconta-1(35),2,4,9,19,21,25(36),26(34),28,30,32-undecaen-13-yl] Acetate

    94. 2,7-(epoxypentadeca(1,11,13)trienimino)benzofuro(4,5-e)pyrido(1,2-a)benzimidazole-1,15(2h)-dione, 25-(acetyloxy)-5,6,21,23-tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-, (2s,16z,18e,20s,21s,22r,23r,24r,25s,26r,27s,28e)-

    95. 5-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)furo[2'',3'':7',8']naphtho[1',2':4,5]imidazo[1,2-a]pyridin-2

    2.4 Create Date
    2006-04-28
    3 Chemical and Physical Properties
    Molecular Weight 785.9 g/mol
    Molecular Formula C43H51N3O11
    XLogP36.9
    Hydrogen Bond Donor Count5
    Hydrogen Bond Acceptor Count12
    Rotatable Bond Count3
    Exact Mass785.35235945 g/mol
    Monoisotopic Mass785.35235945 g/mol
    Topological Polar Surface Area198 Ų
    Heavy Atom Count57
    Formal Charge0
    Complexity1590
    Isotope Atom Count0
    Defined Atom Stereocenter Count9
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count3
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Drug and Medication Information
    4.1 Drug Information
    1 of 2  
    Drug NameXifaxan
    PubMed HealthRifaximin (By mouth)
    Drug ClassesAntibiotic
    Drug LabelXIFAXAN tablets contain rifaximin, a non-aminoglycoside semi-synthetic, nonsystemic antibiotic derived from rifamycin SV. Rifaximin is a structural analog of rifampin. The chemical name for rifaximin is (2 ,16 ,18 ,20 ,21 ,22 ,23 ,24 ,25 ,26 ,27...
    Active IngredientRifaximin
    Dosage FormTablet
    RouteOral
    Strength200mg; 550mg
    Market StatusPrescription
    CompanySalix Pharms

    2 of 2  
    Drug NameXifaxan
    PubMed HealthRifaximin (By mouth)
    Drug ClassesAntibiotic
    Drug LabelXIFAXAN tablets contain rifaximin, a non-aminoglycoside semi-synthetic, nonsystemic antibiotic derived from rifamycin SV. Rifaximin is a structural analog of rifampin. The chemical name for rifaximin is (2 ,16 ,18 ,20 ,21 ,22 ,23 ,24 ,25 ,26 ,27...
    Active IngredientRifaximin
    Dosage FormTablet
    RouteOral
    Strength200mg; 550mg
    Market StatusPrescription
    CompanySalix Pharms

    4.2 Drug Indication

    Rifaximin has multiple indications by the FDA: for the treatment of patients (12 years of age) with traveller's diarrhea caused by noninvasive strains of Escherichia coli; for the reduction of overt hepatic encephalopathy recurrence in patients 18 years of age; and in May 2015 it was approved for irritable bowel syndrome with diarrhea (IBS-D) treatment in adult men and women.

    FDA Label

    5 Pharmacology and Biochemistry
    5.1 Pharmacology

    Rifaximin is a structural analog of rifampin and a non-systemic, gastrointestinal site-specific antibiotic. This non-systemic property of the drug is due to the addition of a pyridoimidazole ring, which renders it non-absorbable. Rifaximin acts by inhibiting bacterial ribonucleic acid (RNA) synthesis and contributes to restore intestinal microflora imbalance. Other studies have also shown rifaximin to be an pregnane X receptor (PXR) activator. As PXR is responsible for inhibiting the proinflammatory transcription factor NF-kappa B (NF-B) and is inhibited in inflammatory bowel disease (IBD), rifaximin was proven to be effective for the treatment of IBS-D.

    5.2 MeSH Pharmacological Classification

    Anti-Bacterial Agents

    Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)

    Gastrointestinal Agents

    Drugs used for their effects on the gastrointestinal system, as to control gastric acidity, regulate gastrointestinal motility and water flow, and improve digestion. (See all compounds classified as Gastrointestinal Agents.)

    5.3 FDA Pharmacological Classification
    5.3.1 Active Moiety
    RIFAXIMIN
    5.3.2 FDA UNII
    L36O5T016N
    5.3.3 Pharmacological Classes
    Rifamycins [CS]; Rifamycin Antibacterial [EPC]
    5.4 ATC Code

    A07AA11

    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

    A - Alimentary tract and metabolism

    A07 - Antidiarrheals, intestinal antiinflammatory/antiinfective agents

    A07A - Intestinal antiinfectives

    A07AA - Antibiotics

    A07AA11 - Rifaximin

    D - Dermatologicals

    D06 - Antibiotics and chemotherapeutics for dermatological use

    D06A - Antibiotics for topical use

    D06AX - Other antibiotics for topical use

    D06AX11 - Rifaximin

    5.5 Absorption, Distribution and Excretion

    Absorption

    Low absorption in both the fasting state and when administered within 30 minutes of a high-fat breakfast.

    Route of Elimination

    In a mass balance study, after administration of 400 mg 14C-rifaximin orally to healthy volunteers, of the 96.94% total recovery, 96.62% of the administered radioactivity was recovered in feces almost exclusively as the unchanged drug and 0.32% was recovered in urine mostly as metabolites with 0.03% as the unchanged drug.Rifaximin accounted for 18% of radioactivity in plasma. This suggests that the absorbed rifaximin undergoes metabolism with minimal renal excretion of the unchanged drug

    5.6 Metabolism/Metabolites

    In vitro drug interactions studies have shown that rifaximin, at concentrations ranging from 2 to 200 ng/mL, did not inhibit human hepatic cytochrome P450 isoenzymes: 1A2, 2A6, 2B6, 2C9, 2C19, 2D6, 2E1, and 3A4. In an in vitro hepa-tocyte induction model, rifaximin was shown to induce cytochrome P450 3A4 (CYP3A4), an isoenzyme which rifampin is known to induce.

    5.7 Biological Half-Life

    Approximately 6 hours.

    5.8 Mechanism of Action

    Rifaximin acts by inhibiting RNA synthesis in susceptible bacteria by binding to the beta-subunit of bacterial deoxyribonucleic acid (DNA)-dependent ribonucleic acid (RNA) polymerase enzyme. This binding blocks translocation, which stops transcription.

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AP","customerAddress":""},{"dataSource":"API Export","activeIngredients":"","year":"2025","qtr":"Q2","strtotime":1751221800,"product":"BATCH NO: 2580001421 TO 422, 2580001955TO 957 CAS NO. 80621-81-4 ACTIVE PHARMACEUTICAL INGREDIENTS RIFAXIMIN","address":"UNIT NO. 3B - 38, 39 AND 40,,3RD F","city":"LBS MARG KURLA WEST,MAHARASHTRA","supplier":"OLON ACTIVE PHARMACEUTICAL INGREDIENTS INDIA PRIVA","supplierCountry":"INDIA","foreign_port":"GENOA","customer":"UNDISCLOSED","customerCountry":"ITALY","quantity":"5006.32","actualQuantity":"5006.32","unit":"KGS","unitRateFc":"218","totalValueFC":"1238612.2","currency":"EURO","unitRateINR":21258.782778567893,"date":"30-Jun-2025","totalValueINR":"106428269.4","totalValueInUsd":"1238612.2","indian_port":"JNPT","hs_no":"29419090","bill_no":"3176291","productDescription":"API","marketType":"REGULATED MARKET","country":"ITALY","selfForZScoreResived":"Pharma Grade","supplierPort":"JNPT","supplierAddress":"UNIT NO. 3B - 38, 39 AND 40,,3RD F, LBS MARG KURLA WEST,MAHARASHTRA","customerAddress":""},{"dataSource":"API Import","activeIngredients":"","year":"2022","qtr":"Q4","strtotime":1669228200,"product":"RIFAXIMIN PH.EUR TEST LIC. 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LTD","supplierCountry":"CHINA","foreign_port":"NA","customer":"ATRA PHARMACEUTICALS LTD","customerCountry":"INDIA","quantity":"10.00","actualQuantity":"10","unit":"KGS","unitRateFc":"280","totalValueFC":"2847.6","currency":"USD","unitRateINR":"23422","date":"02-Mar-2023","totalValueINR":"234220","totalValueInUsd":"2847.6","indian_port":"BOMBAY AIR","hs_no":"29419090","bill_no":"4876158","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"NA","supplierAddress":"","customerAddress":"PLOT NO.H-19,MIDC,WALUJ AURANGABAD"},{"dataSource":"API Import","activeIngredients":"","year":"2023","qtr":"Q2","strtotime":1682533800,"product":"(REJECTED & RE-IMPORT) BATCH: 218002866 RIFAXIMIN (N.C.V.)(FREE REPLACEMENT S\/B NO:5559107 DT. 18.11.2022)","address":"UNIT NO.38, 39 & 40, 3RD FLOOR, PHO PHOENIX MARKET CITY, L.B.S.MARG, KU","city":"MUMBAI","supplier":"ALFASIGMA S P A","supplierCountry":"INDIA","foreign_port":"NA","customer":"OLON ACTIVE PHARMACEUTICAL INGREDIENTS INDIA PRIVA","customerCountry":"INDIA","quantity":"535.83","actualQuantity":"535.832","unit":"KGS","unitRateFc":"209","totalValueFC":"127250.9","currency":"EURO","unitRateINR":"19462.6","date":"27-Apr-2023","totalValueINR":"10428692.33","totalValueInUsd":"127250.9","indian_port":"JNPT","hs_no":"29419090","bill_no":"5705748","productDescription":"Re-Import","marketType":"REGULATED MARKET","country":"INDIA","selfForZScoreResived":"Pharma Grade","supplierPort":"NA","supplierAddress":"","customerAddress":"UNIT NO.38, 39 & 40, 3RD FLOOR, PHO PHOENIX MARKET CITY, L.B.S.MARG, KU"},{"dataSource":"API Import","activeIngredients":"","year":"2023","qtr":"Q2","strtotime":1684348200,"product":"RIFAXIMIN PH EUR LICENCE NO TL WZ 22 002949","address":"H.O.ANJALI COMPLEX,","city":"AURANGABAD","supplier":"LUOHE CHIEF PHARMACEUTICAL CO LTD","supplierCountry":"CHINA","foreign_port":"BEIJING","customer":"RV 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LTD","customerCountry":"INDIA","quantity":"302.72","actualQuantity":"302.72","unit":"KGS","unitRateFc":"129","totalValueFC":"39495.1","currency":"USD","unitRateINR":"10891.3","date":"06-Jun-2024","totalValueINR":"3297024.03","totalValueInUsd":"39495.1","indian_port":"JNPT","hs_no":"29419090","bill_no":"3852601","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"SHANGHAI","supplierAddress":"ROOM 408-410, GONGSHANGLIAN BUILDING, NENJIANG ROAD,YANCHENG DIST-LUOHE CITY, HENAN PROVINCE,P.R.CHINA ., CHINA","customerAddress":"236 OKHLA INDUSTRIAL ESTATE,"}]
    05-Jan-2022
    30-Jun-2025
    KGS
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    South Africa

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    01

    Equity Pharmaceuticals (Pty) Ltd

    United Kingdom
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    Equity Pharmaceuticals (Pty) Ltd

    United Kingdom
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Regulatory Info : Originator

    Registration Country : South Africa

    Rifaximin

    Brand Name : XIFAXAN

    Dosage Form : FCT

    Dosage Strength : 550mg

    Packaging : 56X1mg

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    Regulatory Info : Originator

    Registration Country : South Africa

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    Faran Shimi Pharmaceutical

    Iran
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    Virtual BoothFaran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.

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    Registration Country : Iran

    Rifaximin

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    Dosage Form : Film Coated Tablet

    Dosage Strength : 200MG

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    Registration Country : Iran

    Faran Shimi Pharmaceutical

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    Faran Shimi Pharmaceutical

    Iran
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    Virtual BoothFaran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.

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    Rifaximin

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    Dosage Strength : 200MG

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    Registration Country : Iran

    Faran Shimi Pharmaceutical

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    Faran Shimi Pharmaceutical

    Iran
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    Virtual BoothFaran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.

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    Registration Country : Iran

    Rifaximin

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    Dosage Strength : 550MG

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    Registration Country : Iran

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    Faran Shimi Pharmaceutical

    Iran
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    Virtual BoothFaran Shimi: Leading producer of high-quality APIs & alkaloid opiates, serving major pharmaceutical companies across the Middle East.

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    03

    ALFRED E TIEFENBACHER GmbH & Co KG

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

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    Regulatory Info : EU Dossier Readiness-Q1 2020

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    DOSAGE - TABLET;ORAL - 200MG

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    india-flag.png
    Rifaximin (1 kg - 2 kg) API needed in India [ENA23356]
    A company that focuses on the development of various finished formulations is looking for suppliers of Rifaximin (1 kg - 2 kg) API for development purposes. The suppliers must support this enquiry with USDMF/ CEP & CoA.
    27 Jun 2025

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    27 Jun 2025

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    27 Jun 2025

    Italy.png
    Rifaximin (100 kg - 200 kg) API needed in Italy [ENA22523]
    A CMO that focuses on manufacturing of penicillin and cephalosporins finished formulations is looking for suppliers of Rifaximin (100 kg - 200 kg) API for commercial purposes. The supplier must support this enquiry with DMF & CoA.
    02 Apr 2025

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    02 Apr 2025

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    02 Apr 2025

    China.png
    Rifaximin API needed in China [ENA22020]
    A company that focuses on development, manufacturing and distribution of various FDFs, APIs, intermediates and medical devices is looking for suppliers of Rifaximin API for commercial purposes. The suppliers must support this enquiry with CEP or USDMF (preferred) & CoA.
    10 Feb 2025

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    10 Feb 2025

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    10 Feb 2025

    United_States_of_America.png
    Rifaximin API needed in the U.S.A [ENA21903]
    A CDMO that focuses on the development and manufacturing of various oral, liquid, and semi-solid dosage forms is looking for suppliers of Rifaximin API for development purposes. The suppliers must support this enquiry with USDMF & CoA.
    29 Jan 2025

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    29 Jan 2025

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    29 Jan 2025

    india-flag.png
    BP Grade Rifaximin API needed in India [ENA20794]
    A company that focuses on manufacturing and exporting various finished formulations is looking for suppliers of BP Grade Rifaximin API for development purposes. The suppliers must support this enquiry with DMF & CoA.
    09 Oct 2024

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    09 Oct 2024

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    09 Oct 2024

    Canada.png
    Rifaximin (5 MT - 20 MT) API needed in Canada [ENA20515]
    A company that focuses on development and manufacturing of various finished formulations primarily in gastroenterology, neurology & dermatology is looking for suppliers of Rifaximin (5 MT - 20 MT) API for commercial purposes. The suppliers must support this enquiry with USDMF & CoA.
    11 Sep 2024

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    11 Sep 2024

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    11 Sep 2024

    india-flag.png
    IP Grade Rifaximin (170 kg) API needed in India [ENA19892]
    A company that focuses on manufacturing and marketing of various finished formulations is looking for suppliers of IP Grade Rifaximin (170 kg) API for commercial purposes. The suppliers must support this enquiry with CoA.
    06 Jul 2024

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    06 Jul 2024

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    06 Jul 2024

    india-flag.png
    Rifaximin (10 kg) API needed in India [ENA19696]
    A company that focuses on development and manufacturing of various tablet and capsule finished formulations is looking for suppliers of Rifaximin (10 kg) API for commercial purposes. The suppliers must support this enquiry with DMF, GMP & CoA.
    13 Jun 2024

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    13 Jun 2024

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    13 Jun 2024

    india-flag.png
    Rifaximin (10 kg) API needed in India [ENA18686]
    A company that deals in various pharmaceutical products is looking for suppliers of Rifaximin (10 kg) API for commercial purposes. The suppliers must support this enquiry with CoA.
    25 Nov 2023

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    25 Nov 2023

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    25 Nov 2023

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    Rifaximin (5 g) API needed in India [ENA18405]
    A company that deals in various pharmaceutical products is looking for suppliers of Rifaximin (5 g) API for commercial purposes. The suppliers must support this enquiry with CoA.
    20 Oct 2023

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    20 Oct 2023

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    20 Oct 2023

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    FDF DOSSIERS

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    Tender// Various Finished Dosage Formulations needed in Sweden [ENA18398]
    Region Skane, Group staff purchasing and financial management is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 17-Nov-2023. 1. Rifaximin (550 mg) Tablets. The required quantity is 32,300 units. 2. Alfacalcidol (2 mg/ ml) Injections. The required quantity is 78,500 units.
    19 Oct 2023

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    19 Oct 2023

    MyanmarBurma.png
    Various Finished Dosage Formulations needed in Myanmar [ENA14398]
    A large pharmaceutical company based in India that focuses in various segments such as gynaecology, cardiovascular, diabetology, asthma, paediatric, CNS, GI and NSAIDs is looking for suppliers of Various Finished Dosage Formulations for commercial purpose. The suppliers must support this enquiry with ACTD dossier & WHO-GMP/ PICs. 1. Acotiamide (300 mg) + Rabeprazole (20 mg) Tablets 2. Acotiamide (100 mg) Tablets 3. Flupirtine Maleate (400 mg) SR Tablets 4. Rifaximin (200 mg, 400 mg & 550 mg) Tablets 5. Tirofiban (5 mg/ 100 ml) Injections
    19 Jul 2022

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    19 Jul 2022

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    19 Jul 2022

    SriLanka.png
    Various Finished Dosage Formulations needed in Sri Lanka [ENA14018]
    A leading pharmaceutical company based in India that focused in developing, formulating and commercializing affordable and accessible medicines for urgent medical needs is looking for suppliers of Various Finished Dosage Formulations for commercial purpose. The suppliers must support this enquiry with USFDA or MHRA or TGA. 1. Lactulose (120 ml) Solutions 2. Esomeprazole (20 mg/ 40 mg) Tablets 3. Rifaximin (200 mg/ 550 mg) Tablets 4. Ursodeoxycholic Acid (250 mg) Capsules 5. Flucloxacillin (250 mg/ 500 mg) Capsules
    20 Jun 2022

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    20 Jun 2022

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    20 Jun 2022

    France.png
    Tender// Various Finished Dosage Formulations needed in France [ENA10151]
    Hospitals of Provence is looking for supplies of Various Finished Dosage Formulations. The deadline is 30-April-2021. 1. Cimetidine (200 mg) Effervescent Tablets. The required quantity is 28,220 units. 2. Macrogol (4 g) Powder for Oral Solution. The required quantity is 3,610 units. 3. Rifaximin (550 mg) Tablets. The required quantity is 66,240 units. 4. Glibenclamide (2.5 mg and 5 mg) Oral Form. The required quantity is 3,940 units and 10,010 units respectively. 5. Dapagliflozin (10 mg) Oral Form. The required quantity is 2,910 units. 6. Potassium (25 mg / ml) Oral Form. The required quantity is 1,680 units. 7. Zinc Gluconate (15 mg) Oral Form. The required quantity is 56,130 units. 8. Celiprolol (200 mg) Oral Form. The required quantity is 3,040 units. 9. Metoprolol (100 mg) Oral Form. The required quantity is 2,380 units. 10. Nifedipine (20 mg) Prolonged-Release Tablets. The required quantity is 5,205 units.
    08 Apr 2021

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    08 Apr 2021

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    08 Apr 2021

    CzechRepublic.png
    Tender// Various Finished Dosage Formulations needed in the Czech Republic [ENA10037]
    Fakultní nemocnice Hradec Králové is looking for supplies of Various Finished Dosage Formulations. The deadline is 21-April-2021. 1. Rifaximin (200 mg) Filmed Tablets. The required quantity is 5,860 units. 2. Vancomycin Hydrochloride (500 mg and 1000 mg) Infusion Solution. The required quantity is 15,400 units and 19,160 units respectively. 3. Oxacillin Sodium Monohydrate (1000 mg) Solution for Injection. The required quantity is 164,356 units. 4. Ceftolozane/ Tazobactam (1 g/ 0.5 g) Infusion Solution. The required quantity is 44 units.
    24 Mar 2021

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    24 Mar 2021

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    24 Mar 2021

    Indonesia.png
    Omega-3-Acid Ethyl Ester (1 g) Capsules & Rifaximin (550 mg) Tablets needed in Indonesia [ENA08838]
    A pharmaceutical company that manufactures non-betalactam hard capsules, tablets, powder, semisolid dosage forms for pharmaceuticals, nutraceuticals, and natural-based products is looking for suppliers of Omega-3-Acid Ethyl Ester (1 g) Capsules & Rifaximin (550 mg) Tablets. The required quantity is 3,000,000 units for each.
    19 Oct 2020

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    19 Oct 2020

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    19 Oct 2020

    india-flag.png
    Enquiry// Rifaximin Tablets (400mg) with 3000 units needed in India [ENA01716]
    A well-renowned company with more than 60 years of experience in biotechnology, microbiology and development of chemical processes is looking for the suppliers of Rifaximin Tablets (400mg) with 3000 units. Interested suppliers must contact Rajesh Batra via E-mail: rbatra856@yahoo.co.in or Tel: 9215592586.
    31 Aug 2018

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    31 Aug 2018

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    31 Aug 2018

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    01

    SALIX PHARMS

    RIFAXIMIN

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    BIO Asia-Taiwan
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    SALIX PHARMS

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    Patent Expiration Date : 2027-09-02

    RIFAXIMIN

    US Patent Number : 8193196

    Drug Substance Claim : Y

    Drug Product Claim : Y

    Application Number : 21361

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    Patent Expiration Date : 2027-09-02

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    Patent Expiration Date : 2026-02-27

    RIFAXIMIN

    US Patent Number : 10703763

    Drug Substance Claim :

    Drug Product Claim :

    Application Number : 21361

    Patent Use Code : U-2847

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    Patent Expiration Date : 2026-02-27

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    RIFAXIMIN

    US Patent Number : 10703763

    Drug Substance Claim :

    Drug Product Claim :

    Application Number : 21361

    Patent Use Code : U-2848

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    Patent Use Description :

    Patent Expiration Date : 2026-02-27

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    04

    SALIX PHARMS

    RIFAXIMIN

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    Not Confirmed

    SALIX PHARMS

    U.S.A
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    Not Confirmed

    Patent Expiration Date : 2029-07-24

    RIFAXIMIN

    US Patent Number : 9421195

    Drug Substance Claim :

    Drug Product Claim :

    Application Number : 21361

    Patent Use Code : U-1481

    Delist Requested :

    Patent Use Description : REDUCTION IN RISK OF O...

    Patent Expiration Date : 2029-07-24

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    05

    SALIX PHARMS

    RIFAXIMIN

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    BIO Asia-Taiwan
    Not Confirmed

    SALIX PHARMS

    U.S.A
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    BIO Asia-Taiwan
    Not Confirmed

    Patent Expiration Date : 2027-09-02

    RIFAXIMIN

    US Patent Number : 8193196

    Drug Substance Claim : Y

    Drug Product Claim : Y

    Application Number : 21361

    Patent Use Code : U-1708

    Delist Requested :

    Patent Use Description : TREATMENT OF IRRITABLE...

    Patent Expiration Date : 2027-09-02

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    SALIX PHARMS

    RIFAXIMIN

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    Not Confirmed

    SALIX PHARMS

    U.S.A
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    BIO Asia-Taiwan
    Not Confirmed

    Patent Expiration Date : 2026-02-27

    RIFAXIMIN

    US Patent Number : 8518949

    Drug Substance Claim :

    Drug Product Claim : Y

    Application Number : 21361

    Patent Use Code :

    Delist Requested :

    Patent Use Description :

    Patent Expiration Date : 2026-02-27

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    SALIX PHARMS

    RIFAXIMIN

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    Not Confirmed

    SALIX PHARMS

    U.S.A
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    BIO Asia-Taiwan
    Not Confirmed

    Patent Expiration Date : 2029-02-26

    RIFAXIMIN

    US Patent Number : 11779571

    Drug Substance Claim :

    Drug Product Claim :

    Application Number : 21361

    Patent Use Code : U-3706

    Delist Requested :

    Patent Use Description :

    Patent Expiration Date : 2029-02-26

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    SALIX PHARMS

    RIFAXIMIN

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    Not Confirmed

    SALIX PHARMS

    U.S.A
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    BIO Asia-Taiwan
    Not Confirmed

    Patent Expiration Date : 2026-02-27

    RIFAXIMIN

    US Patent Number : 10703763

    Drug Substance Claim :

    Drug Product Claim :

    Application Number : 21361

    Patent Use Code : U-2847

    Delist Requested :

    Patent Use Description :

    Patent Expiration Date : 2026-02-27

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    09

    SALIX PHARMS

    RIFAXIMIN

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    BIO Asia-Taiwan
    Not Confirmed

    SALIX PHARMS

    U.S.A
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    BIO Asia-Taiwan
    Not Confirmed

    Patent Expiration Date : 2029-10-02

    RIFAXIMIN

    US Patent Number : 8969398

    Drug Substance Claim :

    Drug Product Claim :

    Application Number : 21361

    Patent Use Code : U-1481

    Delist Requested :

    Patent Use Description : REDUCTION IN RISK OF O...

    Patent Expiration Date : 2029-10-02

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    10

    SALIX PHARMS

    RIFAXIMIN

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    Not Confirmed

    SALIX PHARMS

    U.S.A
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    BIO Asia-Taiwan
    Not Confirmed

    Patent Expiration Date : 2029-07-18

    RIFAXIMIN

    US Patent Number : 8309569

    Drug Substance Claim :

    Drug Product Claim :

    Application Number : 21361

    Patent Use Code : U-1708

    Delist Requested : Y

    Patent Use Description : TREATMENT OF IRRITABLE...

    Patent Expiration Date : 2029-07-18

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    ABOUT THIS PAGE

    Looking for 80621-81-4 / Rifaximin API manufacturers, exporters & distributors?

    Rifaximin manufacturers, exporters & distributors 1

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

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

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

    API | Excipient name

    Rifaximin

    Synonyms

    Rifaxidin, Rifacol, 80621-81-4, Rifamycin l 105, Xifaxan, Rifamycin l 105sv

    Cas Number

    80621-81-4

    Unique Ingredient Identifier (UNII)

    L36O5T016N

    About Rifaximin

    A synthetic rifamycin derivative and anti-bacterial agent that is used for the treatment of GASTROENTERITIS caused by ESCHERICHIA COLI INFECTIONS. It may also be used in the treatment of HEPATIC ENCEPHALOPATHY.

    Normix Manufacturers

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

    Normix Suppliers

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

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

    Normix USDMF

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

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

    click here to find a list of Normix suppliers with USDMF on PharmaCompass.

    Normix JDMF

    The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

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

    Normix KDMF

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

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

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

    click here to find a list of Normix suppliers with KDMF on PharmaCompass.

    Normix CEP

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

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

    Normix WC

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

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

    Normix 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 Normix as an active pharmaceutical ingredient (API).

    Finished drug products

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

    click here to find a list of Normix suppliers with NDC on PharmaCompass.

    Normix GMP

    Normix 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 Normix 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 Normix GMP manufacturer or Normix GMP API supplier for your needs.

    Normix CoA

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

    Normix CoA mostly includes findings from lab analyses of a specific batch. For each Normix 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.

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