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1. Cerubidine
2. Dauno Rubidomycine
3. Dauno-rubidomycine
4. Daunoblastin
5. Daunoblastine
6. Daunomycin
7. Daunorubicin
8. Hydrochloride, Daunorubicin
9. Nsc 82151
10. Nsc-82151
11. Nsc82151
12. Rubidomycin
13. Rubomycin
1. 23541-50-6
2. Daunorubicin Hcl
3. Daunomycin Hydrochloride
4. Cerubidine
5. Rubidomycin Hydrochloride
6. Rp 13057 Hydrochloride
7. Daunomycin Hcl
8. Ndc 0082-4155
9. Rp-13057 Hydrochloride
10. Daunorubicin (hydrochloride)
11. Daunoblastin
12. Ondena
13. Rubomycin
14. Fi 6339 [as The Base]
15. Daunomycin, Hydrochloride
16. Ud984i04lz
17. Daunorubicin (as Hydrochloride)
18. (8s,10s)-8-acetyl-10-(((2r,4s,5s,6s)-4-amino-5-hydroxy-6-methyltetrahydro-2h-pyran-2-yl)oxy)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione Hydrochloride
19. Fi 6339 Hydrochloride
20. Fi-6339 Hydrochloride
21. Daunoxome
22. (8s-cis)-8-acetyl-10-((3-amino-2,3,6-trideoxy-alpha-l-lyxo-hexopyranosyl)oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-naphthacenedione Hydrochloride
23. Daunoblastina
24. Nsc-82151
25. Rp 13057 [as The Base]
26. Daunomycin Chlorohydrate
27. Mls000069508
28. Mfcd04974507
29. Rp 13057 [as The Base)
30. Ccris 915
31. Mls001336042
32. Smr000058559
33. Einecs 245-723-4
34. Unii-ud984i04lz
35. C27h29no10.hcl
36. Daunorubicin Hcl (daunomycin Hcl)
37. Ai3-44887
38. Sr-01000000033
39. Sr-05000001600
40. Cerubidine (tn)
41. Daunorubicin,(s)
42. Daunorubicin Hydrochloride(bicins)
43. (8s,10s)-8-acetyl-10-((2r,4s,5s,6s)-4-amino-5-hydroxy-6-methyltetrahydro-2h-pyran-2-yloxy)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione Hydrochloride
44. (8s,10s)-8-acetyl-10-[[(2r,4s,5s,6s)-4-amino-5-hydroxy-6-methyltetrahydro-2h-pyran-2-yl]oxy]-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione Hydrochloride
45. Smr000768722
46. Daunorubicin Hydrochloride [usan:usp:jan]
47. (7s,9s)-9-acetyl-7-[(2r,4s,5s,6s)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy-6,9,11-trihydroxy-4-methoxy-8,10-dihydro-7h-tetracene-5,12-dione;hydrochloride
48. Daunorubicin Hcl- Bio-x
49. Schembl4444
50. Cas-23541-50-6
51. Chembl1563
52. Dsstox_cid_13382
53. Dsstox_rid_79068
54. Dsstox_gsid_33382
55. (1s,3s)-3-acetyl-1,2,3,4,6,11-hexahydro-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1-naphthacenyl 3-amino-2,3,6-trideoxy-alpha-l-lyxo-hexopyranoside Hydrochloride
56. Mls002222263
57. Dtxsid0033382
58. Chebi:31456
59. (8s,10s)-8-acetyl-10-[(3-amino-2,3,6-trideoxy-?-l-lyxo-hexopyransoyl)oxy]-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-5,12-naphthacenedione Hydrochloride
60. Ex-a2649
61. Tox21_201159
62. Ccg-39942
63. S3035
64. Akos015920259
65. Cs-1271
66. Daunorubicin Hydrochloride (jp17/usp)
67. Daunorubicin Hydrochloride [mi]
68. Ks-5149
69. Daunorubicin Hydrochloride [jan]
70. Daunorubicin Hydrochloride [usan]
71. Ncgc00024246-03
72. Ncgc00258711-01
73. 5,12-naphthacenedione, 8-acetyl-10-((3-amino-2,3,6-trideoxy-alpha-l-lyxo-hexopyranosyl))oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-, (8s-cis)-, Hydrochloride
74. 5,12-naphthacenedione, 8-acetyl-10-((3-amino-2,3,6-trideoxy-alpha-l-lyxo-hexopyranosyl)oxy)-7,8,9,10-tetrahydro-6,8,11-trhydroxy-1-methoxy-, Hydrochloride, (8s,10s)-
75. 5,12-naphthacenedione, 8-acetyl-10-((3-amino-2,3,6-trideoxy-alpha-l-lyxo-hexopyranosyl)oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-, (8s-cis)-, Hydrochloride
76. Bd164356
77. Daunorubicin Hydrochloride [mart.]
78. Daunorubicin Hydrochloride [vandf]
79. Hy-13062
80. Daunorubicin Hydrochloride [usp-rs]
81. Daunorubicin Hydrochloride [who-dd]
82. Daunorubicin Hydrochloride, >=90% (hplc)
83. D01264
84. Daunorubicin Hydrochloride [orange Book]
85. Wp900 Hydrochloride, >=95% (hplc), Solid
86. Daunorubicin Hydrochloride [ep Monograph]
87. Daunorubicin Hydrochloride [usp Impurity]
88. 541d506
89. A816764
90. Daunorubicin Hydrochloride [usp Monograph]
91. Sr-01000000033-6
92. Sr-05000001600-3
93. Q27291034
94. Daunorubicin Hydrochloride, Meets Usp Testing Specifications
95. Daunorubicin Hydrochloride; Rp 13057 Hydrochloride; Daunomycin
96. Daunorubicin Hydrochloride, European Pharmacopoeia (ep) Reference Standard
97. Daunorubicin Hydrochloride, United States Pharmacopeia (usp) Reference Standard
98. (1s,3s)-3-acetyl-1,2,3,4,6,11-hexahydro-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1-naphthacenyl 3-amino-2,3,6-trideoxy-.alpha.-l-lyxo-hexopyranoside Hydrochloride
99. (1s,3s)-3-acetyl-3,5,12-trihydroxy-10-methoxy-6,11-dioxo-1,2,3,4,6,11-hexahydrotetracen-1-yl 3-amino-2,3,6-trideoxy-a-l-lyxo-hexopyranoside Hydrochloride
100. (8s,10s)-8-acetyl-10-(((2r,4s,5s,6s)-4-amino-5-hydroxy-6-methyltetrahydro-2h-pyran-2-yl)oxy)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dionehydrochloride
101. 5,12-naphthacenedione, 8-acetyl-10-((3-amino-2,3,6-trideoxy-.alpha.-l-lyxo-hexopyranosyl))oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-, (8s-cis)-, Hydrochloride
102. 5,12-naphthacenedione, 8-acetyl-10-((3-amino-2,3,6-trideoxy-alpha-l-lyxo-hexopyranosyl)oxy)-7,8,9,10-tetrahydro-6,8,11-trihydroxy-1-methoxy-, Hydrochloride, (8s,10s)-
103. Daunorubicin Hydrochloride;(8s,10s)-8-acetyl-10-[[(2r,4s,5s,6s)-4-amino-5-hydroxy-6-methyltetrahydro-2h-pyran-2-yl]oxy]-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione Hydrochloride
Molecular Weight | 564.0 g/mol |
---|---|
Molecular Formula | C27H30ClNO10 |
Hydrogen Bond Donor Count | 6 |
Hydrogen Bond Acceptor Count | 11 |
Rotatable Bond Count | 4 |
Exact Mass | 563.1558238 g/mol |
Monoisotopic Mass | 563.1558238 g/mol |
Topological Polar Surface Area | 186 Ų |
Heavy Atom Count | 39 |
Formal Charge | 0 |
Complexity | 960 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 6 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
1 of 2 | |
---|---|
Drug Name | Daunorubicin hydrochloride |
Drug Label | Daunorubicin Hydrochloride Injection consists of the hydrochloride salt of an anthracycline cytotoxic antibiotic produced by a strain of Streptomyces coeruleorubidus. It is provided as a deep red sterile liquid in vials for intravenous administration... |
Active Ingredient | Daunorubicin hydrochloride |
Dosage Form | Injectable |
Route | Injection |
Strength | eq 5mg base/ml; eq 20mg base/vial; eq 5mg base/vial |
Market Status | Prescription |
Company | Fresenius Kabi Usa; Teva Pharms Usa; Eurohlth Intl |
2 of 2 | |
---|---|
Drug Name | Daunorubicin hydrochloride |
Drug Label | Daunorubicin Hydrochloride Injection consists of the hydrochloride salt of an anthracycline cytotoxic antibiotic produced by a strain of Streptomyces coeruleorubidus. It is provided as a deep red sterile liquid in vials for intravenous administration... |
Active Ingredient | Daunorubicin hydrochloride |
Dosage Form | Injectable |
Route | Injection |
Strength | eq 5mg base/ml; eq 20mg base/vial; eq 5mg base/vial |
Market Status | Prescription |
Company | Fresenius Kabi Usa; Teva Pharms Usa; Eurohlth Intl |
Topoisomerase II Inhibitors
Compounds that inhibit the activity of DNA TOPOISOMERASE II. Included in this category are a variety of ANTINEOPLASTIC AGENTS which target the eukaryotic form of topoisomerase II and ANTIBACTERIAL AGENTS which target the prokaryotic form of topoisomerase II. (See all compounds classified as Topoisomerase II Inhibitors.)
Antibiotics, Antineoplastic
Chemical substances, produced by microorganisms, inhibiting or preventing the proliferation of neoplasms. (See all compounds classified as Antibiotics, Antineoplastic.)
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PharmaCompass offers a list of Daunorubicin HCl 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 Daunorubicin HCl manufacturer or Daunorubicin HCl supplier for your needs.
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A Daunomycin HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Daunomycin HCl, including repackagers and relabelers. The FDA regulates Daunomycin HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Daunomycin HCl API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Daunomycin HCl supplier is an individual or a company that provides Daunomycin HCl active pharmaceutical ingredient (API) or Daunomycin HCl finished formulations upon request. The Daunomycin HCl suppliers may include Daunomycin HCl API manufacturers, exporters, distributors and traders.
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A Daunomycin HCl DMF (Drug Master File) is a document detailing the whole manufacturing process of Daunomycin HCl active pharmaceutical ingredient (API) in detail. Different forms of Daunomycin HCl DMFs exist exist since differing nations have different regulations, such as Daunomycin HCl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Daunomycin HCl DMF submitted to regulatory agencies in the US is known as a USDMF. Daunomycin HCl USDMF includes data on Daunomycin HCl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Daunomycin HCl USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 Daunomycin HCl Drug Master File in Japan (Daunomycin HCl JDMF) empowers Daunomycin HCl 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 Daunomycin HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Daunomycin HCl JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Daunomycin HCl Drug Master File in Korea (Daunomycin HCl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Daunomycin HCl. The MFDS reviews the Daunomycin HCl KDMF as part of the drug registration process and uses the information provided in the Daunomycin HCl KDMF to evaluate the safety and efficacy of the drug.
After submitting a Daunomycin HCl 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 Daunomycin HCl API can apply through the Korea Drug Master File (KDMF).
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A Daunomycin HCl CEP of the European Pharmacopoeia monograph is often referred to as a Daunomycin HCl Certificate of Suitability (COS). The purpose of a Daunomycin HCl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Daunomycin HCl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Daunomycin HCl to their clients by showing that a Daunomycin HCl CEP has been issued for it. The manufacturer submits a Daunomycin HCl CEP (COS) as part of the market authorization procedure, and it takes on the role of a Daunomycin HCl CEP holder for the record. Additionally, the data presented in the Daunomycin HCl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Daunomycin HCl DMF.
A Daunomycin HCl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Daunomycin HCl CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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A Daunomycin HCl written confirmation (Daunomycin HCl WC) is an official document issued by a regulatory agency to a Daunomycin HCl manufacturer, verifying that the manufacturing facility of a Daunomycin HCl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Daunomycin HCl APIs or Daunomycin HCl finished pharmaceutical products to another nation, regulatory agencies frequently require a Daunomycin HCl WC (written confirmation) as part of the regulatory process.
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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 Daunomycin HCl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Daunomycin HCl 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 Daunomycin HCl 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 Daunomycin HCl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Daunomycin HCl NDC to their finished compounded human drug products, they may choose to do so.
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Daunomycin HCl 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 Daunomycin HCl 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 Daunomycin HCl GMP manufacturer or Daunomycin HCl GMP API supplier for your needs.
A Daunomycin HCl CoA (Certificate of Analysis) is a formal document that attests to Daunomycin HCl's compliance with Daunomycin HCl specifications and serves as a tool for batch-level quality control.
Daunomycin HCl CoA mostly includes findings from lab analyses of a specific batch. For each Daunomycin HCl 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.
Daunomycin HCl may be tested according to a variety of international standards, such as European Pharmacopoeia (Daunomycin HCl EP), Daunomycin HCl JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Daunomycin HCl USP).