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1. Ancef
2. Cefamedin
3. Cefamezine
4. Cefazolin
5. Cephamezine
6. Cephazolin
7. Cephazolin Sodium
8. Cephazolin, Sodium
9. Gramaxin
10. Kefzol
11. Sodium Cephazolin
12. Sodium, Cefazolin
13. Sodium, Cephazolin
14. Totacef
1. Cefazolin Sodium Salt
2. 27164-46-1
3. Cefazoline Sodium
4. Ancef
5. Cefazil
6. Totacef
7. Kefzol
8. Sodium Cephazolin
9. Cefamedin
10. Gramaxin
11. Zolicef
12. Sodium Cefazolin
13. Cefacidal
14. Cephazolin Sodium
15. Cefazolin (sodium)
16. Monosodium Cefazolin
17. Sk&f 41558
18. Cefazolin Injection
19. Cefazolin And Dextrose
20. Cefazina
21. Firmacef
22. Liviclina
23. Atirin
24. Acef
25. Chebi:3483
26. Mls000028706
27. Nsc-291561
28. P380m0454z
29. Biazolina
30. Smr000058708
31. Skf 41558
32. Sk&f-41558
33. Sodium Cez
34. Cefazolin Sodium 100 Microg/ml In Acetonitrile/water
35. Ancef In Plastic Container
36. Cefabiozim
37. Cefalomicina
38. Lampocef
39. Neofazol
40. Zolisint
41. Recef
42. Zolin
43. Bor-cefazol
44. Cez Sodium
45. 5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-7-(((1h-tetrazol-1-yl)acetyl)amino)-, Monosodium Salt (6r-trans)-
46. Monosodium (6r,7r)-3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-7-(2-(1h-tetrazol-1-yl)acetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylate
47. Lilly 46083
48. Unii-p380m0454z
49. Cefazolin Sodium [usan:usp:jan]
50. Sodium;(6r,7r)-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-8-oxo-7-[[2-(tetrazol-1-yl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
51. Prestwick_975
52. Einecs 248-278-4
53. Monosodium Cephazolin
54. Mfcd00056883
55. Ancef (tn)
56. Nsc 291561
57. Opera_id_1323
58. Ancef In Dextrose 5% In Plastic Container
59. Schembl40735
60. Spectrum1500164
61. Cefazolin Sodium [jan]
62. Cefazolin Sodium (jp17/usp)
63. Sodium Cez; Skf-41558
64. Cefazolin Sodium [usan]
65. Cefazolin Sodium [vandf]
66. Chembl1200523
67. Hms500a16
68. Ancef In Sodium Chloride 0.9% In Plastic Container
69. Cefazolin Sodium [mart.]
70. Cefazolin Sodium [who-dd]
71. Dtxsid901015786
72. Hms1570c14
73. Hms1920k07
74. Hms2091a10
75. Hms2097c14
76. Hms2230i22
77. Hms3260h10
78. Hms3714c14
79. Cefazolin Sodium Salt [mi]
80. Hy-b1078
81. Tox21_500274
82. Bdbm50247885
83. Ccg-40011
84. S4595
85. Akos015895533
86. Cefazolin Sodium [orange Book]
87. Cefazolin Sodium [ep Monograph]
88. Cs-4634
89. Lp00274
90. Cefazolin Sodium [usp Monograph]
91. Cefazolin Sodium Salt, 89.1-110.1%
92. Ncgc00093731-01
93. Ncgc00260959-01
94. 3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-7-(2-(1h-tetrazol-1-yl)acetamido)-3-cephem-4-carboxylate
95. Ac-13166
96. Ac-31729
97. As-12230
98. Sodium (6r,7r)-3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-7-(2-(1h-tetrazol-1-yl)acetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylate
99. Eu-0100274
100. C 5020
101. C-2465
102. C08098
103. D00905
104. Q27106104
105. Cefazolin Sodium Salt, Antibiotic For Culture Media Use Only
106. 5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic Acid, 3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-7-(((1h-tetrazol-1-yl)acetyl)amino)-, (6r-trans)-, Sodium Salt
107. 5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid, 3-[[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-8-oxo-7-[[2-(1h-tetrazol-1-yl)acetyl]amino]-, Sodium Salt, (6r,7r)- (1:1)
108. 5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid, 3-[[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-8-oxo-7-[[2-(1h-tetrazol-1-yl)acetyl]amino]-,(6r,7r)-,sodium
109. Sodium (6r,7r)-3-{[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl}-8-oxo-7-[(1h-tetrazol-1-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
110. Sodium (6r,7r)-7-(2-(1h-tetrazol-1-yl)acetamido)-3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
111. Sodium (6r,7r)-7-(2-(1h-tetrazol-1-yl)acetamido)-3-((5-methyl-1,3,4-thiadiazol-2-ylthio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
112. Sodium (6r-trans)-3-(((5-methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-7-(1h-tetrazol-1-ylacetamido)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylate
113. Sodium 3-{[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl}-7beta-[(1h-tetrazol-1-ylacetyl)amino]-3,4-didehydrocepham-4-carboxylate
114. Sodium 7beta-(1h-tetrazol-1-yl)acetamido-3-(2-methyl-1,3,4-thiadiazol-5-yl)thiomethyl-3-cephem-4-carboxylate
115. Sodium 7beta-[2-(1h-tetrazol-1-yl)-acetamido]-3-(2-methyl-1,3,4-thiadiazol-5-yl)thiomethyl-3-cephem-4-carboxylate
116. Sodium 7beta-[2-(1h-tetrazol-1-yl)acetamido]-3-(2-methyl-1,3,4-thiadiazol-5-yl)thiomethyl-3-cephem-4-carboxylate
| Molecular Weight | 476.5 g/mol |
|---|---|
| Molecular Formula | C14H13N8NaO4S3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 7 |
| Exact Mass | 476.01195873 g/mol |
| Monoisotopic Mass | 476.01195873 g/mol |
| Topological Polar Surface Area | 238 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 746 |
| 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 8 | |
|---|---|
| Drug Name | Ancef in plastic container |
| Active Ingredient | Cefazolin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 20mg base/ml; eq 10mg base/ml |
| Market Status | Prescription |
| Company | Baxter Hlthcare |
| 2 of 8 | |
|---|---|
| Drug Name | Cefazolin and dextrose |
| Active Ingredient | Cefazolin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 2gm base/vial; eq 1gm base/vial |
| Market Status | Prescription |
| Company | B Braun |
| 3 of 8 | |
|---|---|
| Drug Name | Cefazolin sodium |
| Drug Label | CEFAZOLIN FOR INJECTION is a semi-synthetic cephalosporin for parenteral administration. It is the sodium salt of 3-{[(5-methyl-1,3,4-thiadiazol-2-yl)thio]-methyl}-8-oxo-7-[2-(1H-tetrazol-1-yl)acetamido]-5-thia-1-azabicyclo [4.2.0]oct-2-ene-2-carboxy... |
| Active Ingredient | Cefazolin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 20gm base/vial; eq 100gm base/vial; eq 500mg base/vial; eq 10gm base/vial; eq 300gm base/vial; eq 1gm base/vial |
| Market Status | Prescription |
| Company | Acs Dobfar; Hospira; Steri Pharma; Hikma Farmaceutica; Samson Medcl; Sandoz |
| 4 of 8 | |
|---|---|
| Drug Name | Kefzol |
| Active Ingredient | Cefazolin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 500mg base/vial; eq 10gm base/vial; eq 1gm base/vial |
| Market Status | Prescription |
| Company | Acs Dobfar |
| 5 of 8 | |
|---|---|
| Drug Name | Ancef in plastic container |
| Active Ingredient | Cefazolin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 20mg base/ml; eq 10mg base/ml |
| Market Status | Prescription |
| Company | Baxter Hlthcare |
| 6 of 8 | |
|---|---|
| Drug Name | Cefazolin and dextrose |
| Active Ingredient | Cefazolin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 2gm base/vial; eq 1gm base/vial |
| Market Status | Prescription |
| Company | B Braun |
| 7 of 8 | |
|---|---|
| Drug Name | Cefazolin sodium |
| Drug Label | CEFAZOLIN FOR INJECTION is a semi-synthetic cephalosporin for parenteral administration. It is the sodium salt of 3-{[(5-methyl-1,3,4-thiadiazol-2-yl)thio]-methyl}-8-oxo-7-[2-(1H-tetrazol-1-yl)acetamido]-5-thia-1-azabicyclo [4.2.0]oct-2-ene-2-carboxy... |
| Active Ingredient | Cefazolin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 20gm base/vial; eq 100gm base/vial; eq 500mg base/vial; eq 10gm base/vial; eq 300gm base/vial; eq 1gm base/vial |
| Market Status | Prescription |
| Company | Acs Dobfar; Hospira; Steri Pharma; Hikma Farmaceutica; Samson Medcl; Sandoz |
| 8 of 8 | |
|---|---|
| Drug Name | Kefzol |
| Active Ingredient | Cefazolin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 500mg base/vial; eq 10gm base/vial; eq 1gm base/vial |
| Market Status | Prescription |
| Company | Acs Dobfar |
Anti-Bacterial Agents
Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)
API SUPPLIERS
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USDMF
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]CEP/COS
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Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - SOLUTION;INTRAVENOUS - EQ 1GM BASE/5...DOSAGE - SOLUTION;INTRAVENOUS - EQ 1GM BASE/50ML (EQ 20MG BASE/ML)
USFDA APPLICATION NUMBER - 207131
DOSAGE - SOLUTION;INTRAVENOUS - EQ 2GM BASE/1...DOSAGE - SOLUTION;INTRAVENOUS - EQ 2GM BASE/100ML (EQ 20MG BASE/ML)
USFDA APPLICATION NUMBER - 207131
DOSAGE - SOLUTION;INTRAVENOUS - EQ 3GM BASE/1...DOSAGE - SOLUTION;INTRAVENOUS - EQ 3GM BASE/150ML (EQ 20MG BASE/ML)
USFDA APPLICATION NUMBER - 207131
DOSAGE - INJECTABLE;INJECTION - EQ 1GM BASE/V...DOSAGE - INJECTABLE;INJECTION - EQ 1GM BASE/VIAL
USFDA APPLICATION NUMBER - 50779
DOSAGE - INJECTABLE;INJECTION - EQ 2GM BASE/V...DOSAGE - INJECTABLE;INJECTION - EQ 2GM BASE/VIAL
USFDA APPLICATION NUMBER - 50779
DOSAGE - INJECTABLE;INJECTION - EQ 3GM BASE/V...DOSAGE - INJECTABLE;INJECTION - EQ 3GM BASE/VIAL
USFDA APPLICATION NUMBER - 50779
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ABOUT THIS PAGE
95
PharmaCompass offers a list of Cefazolin Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cefazolin Sodium manufacturer or Cefazolin Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefazolin Sodium manufacturer or Cefazolin Sodium supplier.
PharmaCompass also assists you with knowing the Cefazolin Sodium API Price utilized in the formulation of products. Cefazolin Sodium API Price is not always fixed or binding as the Cefazolin Sodium Price is obtained through a variety of data sources. The Cefazolin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zolin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolin, including repackagers and relabelers. The FDA regulates Zolin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolin 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 Zolin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zolin supplier is an individual or a company that provides Zolin active pharmaceutical ingredient (API) or Zolin finished formulations upon request. The Zolin suppliers may include Zolin API manufacturers, exporters, distributors and traders.
click here to find a list of Zolin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zolin DMF (Drug Master File) is a document detailing the whole manufacturing process of Zolin active pharmaceutical ingredient (API) in detail. Different forms of Zolin DMFs exist exist since differing nations have different regulations, such as Zolin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zolin DMF submitted to regulatory agencies in the US is known as a USDMF. Zolin USDMF includes data on Zolin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zolin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zolin 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 Zolin Drug Master File in Japan (Zolin JDMF) empowers Zolin 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 Zolin JDMF during the approval evaluation for pharmaceutical products. At the time of Zolin 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 Zolin suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Zolin Drug Master File in Korea (Zolin KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Zolin. The MFDS reviews the Zolin KDMF as part of the drug registration process and uses the information provided in the Zolin KDMF to evaluate the safety and efficacy of the drug.
After submitting a Zolin 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 Zolin API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Zolin suppliers with KDMF on PharmaCompass.
A Zolin CEP of the European Pharmacopoeia monograph is often referred to as a Zolin Certificate of Suitability (COS). The purpose of a Zolin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zolin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zolin to their clients by showing that a Zolin CEP has been issued for it. The manufacturer submits a Zolin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zolin CEP holder for the record. Additionally, the data presented in the Zolin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zolin DMF.
A Zolin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zolin 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 Zolin suppliers with CEP (COS) on PharmaCompass.
A Zolin written confirmation (Zolin WC) is an official document issued by a regulatory agency to a Zolin manufacturer, verifying that the manufacturing facility of a Zolin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zolin APIs or Zolin finished pharmaceutical products to another nation, regulatory agencies frequently require a Zolin WC (written confirmation) as part of the regulatory process.
click here to find a list of Zolin 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 Zolin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zolin 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 Zolin 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 Zolin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zolin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zolin suppliers with NDC on PharmaCompass.
Zolin 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 Zolin 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 Zolin GMP manufacturer or Zolin GMP API supplier for your needs.
A Zolin CoA (Certificate of Analysis) is a formal document that attests to Zolin's compliance with Zolin specifications and serves as a tool for batch-level quality control.
Zolin CoA mostly includes findings from lab analyses of a specific batch. For each Zolin 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.
Zolin may be tested according to a variety of international standards, such as European Pharmacopoeia (Zolin EP), Zolin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zolin USP).
