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1. Amcill
2. Aminobenzyl Penicillin
3. Aminobenzylpenicillin
4. Ampicillin
5. Ampicillin Trihydrate
6. Antibiotic Ks R1
7. Antibiotic Ks-r1
8. Ks-r1, Antibiotic
9. Omnipen
10. Penicillin, Aminobenzyl
11. Pentrexyl
12. Polycillin
13. Sodium, Ampicillin
14. Trihydrate, Ampicillin
15. Ukapen
1. 200-708-1
2. 69-52-3
3. Ampicillin Sodium Salt
4. Sodium Ampicillin
5. Citteral
6. Domicillin
7. Penialmen
8. Ampicillin Natrium
9. Omnipen
10. Penbritin
11. Totacillin
12. Ampicillin (sodium)
13. Austrapen
14. Polycillin-n
15. Sodium D-(-)-alpha-aminobenzylpenicillin
16. Totacillin-n
17. Penbritin-s
18. Omnipen-n
19. Ampicillin (as Sodium)
20. Jfn36l5s8k
21. Mls000028726
22. D(-)-alpha-aminobenzylpenicillin Sodium Salt
23. Chebi:34535
24. Nsc-755864
25. Smr000059229
26. Monosodium D-(-)-6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate
27. Sodium (2s,5r,6r)-6-((r)-2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
28. Ampicillinsodium
29. Binotal Sodium
30. Sodium Binotal
31. Principen/n
32. Amcill-s
33. Alpen-n
34. Sodium;(2s,5r,6r)-6-[[(2r)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
35. Sodium P-50
36. Mfcd00064313
37. Pen A/n
38. Unii-jfn36l5s8k
39. Ampiplus Simplex
40. Viccillin (tn)
41. Prestwick_822
42. Ampicillin Sodium [usan:usp:jan]
43. Einecs 200-708-1
44. Ampicillinum Natricum
45. Omnipen-n (tn)
46. Ampicillin Sodium Salt, Cell Culture Grade
47. Opera_id_709
48. (2s,5r,6r)-6-[[(2r)-2-amino-2-phenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt
49. Ampicillinsodiumsalt
50. Ampicillin Sodium, Sterile
51. Schembl40521
52. Spectrum1500123
53. Ampicillin Sodium [jan]
54. Ampicillin Sodium (jp17/usp)
55. Ampicillin Sodium [usan]
56. Chembl1200758
57. Hms501h08
58. Hy-b0522a
59. Ampicillin Sodium [vandf]
60. Dtxsid60988759
61. Ampicillin Sodium [mart.]
62. Hms1920c21
63. Hms2091i21
64. Hms2232j12
65. Ampicillin Sodium [usp-rs]
66. Ampicillin Sodium [who-dd]
67. Ampicillin Sodium [who-ip]
68. Ampicillin Sodium Salt [mi]
69. Ccg-39691
70. S3170
71. Akos015967315
72. Akos025147373
73. Ampicillin Sodium [green Book]
74. Ac-8806
75. Ampicillin Sodium [orange Book]
76. Nsc 755864
77. Ampicillin Sodium [ep Monograph]
78. Ampicillin Sodium [usp Monograph]
79. D-(-)-alpha-aminobenzylpenicillin &sdot
80. 4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-((aminophenylacetyl)amino)-3,3-dimethyl-7-oxo-, Monosodium Salt, (2s-(2alpha,5alpha,6beta(s*)))-
81. Ba166035
82. Monosodium (2s,5r,6r)-6-((r)-2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate
83. D-(-)-a-aminobenzylpenicillin Sodium Salt
84. Ampicillin Sodium, Sterile [who-ip]
85. Ampicillinum Natricum [who-ip Latin]
86. Sw220219-1
87. A-7700
88. D02119
89. A836527
90. Ampicillin Sodium (non-injectable) [who-ip]
91. Q27116136
92. Ampicillin Sodium Salt, Antibiotic For Culture Media Use Only
93. Sodium 6beta-[(2r)-2-amino-2-phenylacetamido]-2,2-dimethylpenam-3alpha-carboxylate
94. (2s,5r,6r)-6-[[(2r)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid, Sodium Salt (1:1)
95. 4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-((aminophenylacetyl)amino)-3,3-dimethyl-7-oxo-, Monosodium Salt, (2s-(2.alpha.,5.alpha.,6.beta.(s*)))-
96. 4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic Acid, 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-, Sodium Salt, D-(-)-
97. 6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-,sodiumsalt,d-(-)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid
98. Sodium (2s-(2alpha,5alpha,6beta(s*)))-6-(aminophenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylate
99. Sodium(2s,5r,6r)-6-((r)-2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
| Molecular Weight | 371.4 g/mol |
|---|---|
| Molecular Formula | C16H18N3NaO4S |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 4 |
| Exact Mass | 371.09157152 g/mol |
| Monoisotopic Mass | 371.09157152 g/mol |
| Topological Polar Surface Area | 141 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 568 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| 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 | Ampicillin sodium |
| Drug Label | Ampicillin for Injection, USP the monosodium salt of [2S-[2,5,6(S*)]]-6- [(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-4thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, is a synthetic penicillin for intramuscular or intravenous use. The pha... |
| Active Ingredient | Ampicillin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 2gm base/vial; eq 125mg base/vial; eq 500mg base/vial; eq 10gm base/vial; eq 250mg base/vial; eq 1gm base/vial |
| Market Status | Prescription |
| Company | Istituto Bio Ita Spa; Antibiotice; Hanford Gc; Acs Dobfar Spa; Aurobindo Pharma; Strides Arcolab; Sandoz; Agila Speclts |
| 2 of 2 | |
|---|---|
| Drug Name | Ampicillin sodium |
| Drug Label | Ampicillin for Injection, USP the monosodium salt of [2S-[2,5,6(S*)]]-6- [(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-4thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, is a synthetic penicillin for intramuscular or intravenous use. The pha... |
| Active Ingredient | Ampicillin sodium |
| Dosage Form | Injectable |
| Route | Injection |
| Strength | eq 2gm base/vial; eq 125mg base/vial; eq 500mg base/vial; eq 10gm base/vial; eq 250mg base/vial; eq 1gm base/vial |
| Market Status | Prescription |
| Company | Istituto Bio Ita Spa; Antibiotice; Hanford Gc; Acs Dobfar Spa; Aurobindo Pharma; Strides Arcolab; Sandoz; Agila Speclts |
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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PharmaCompass offers a list of Ampicillin 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 Ampicillin Sodium manufacturer or Ampicillin Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ampicillin Sodium manufacturer or Ampicillin Sodium supplier.
PharmaCompass also assists you with knowing the Ampicillin Sodium API Price utilized in the formulation of products. Ampicillin Sodium API Price is not always fixed or binding as the Ampicillin Sodium Price is obtained through a variety of data sources. The Ampicillin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A UNASYN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNASYN, including repackagers and relabelers. The FDA regulates UNASYN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNASYN 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 UNASYN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A UNASYN supplier is an individual or a company that provides UNASYN active pharmaceutical ingredient (API) or UNASYN finished formulations upon request. The UNASYN suppliers may include UNASYN API manufacturers, exporters, distributors and traders.
click here to find a list of UNASYN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A UNASYN DMF (Drug Master File) is a document detailing the whole manufacturing process of UNASYN active pharmaceutical ingredient (API) in detail. Different forms of UNASYN DMFs exist exist since differing nations have different regulations, such as UNASYN USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A UNASYN DMF submitted to regulatory agencies in the US is known as a USDMF. UNASYN USDMF includes data on UNASYN's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The UNASYN USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of UNASYN 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 UNASYN Drug Master File in Japan (UNASYN JDMF) empowers UNASYN 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 UNASYN JDMF during the approval evaluation for pharmaceutical products. At the time of UNASYN 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 UNASYN 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 UNASYN Drug Master File in Korea (UNASYN KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of UNASYN. The MFDS reviews the UNASYN KDMF as part of the drug registration process and uses the information provided in the UNASYN KDMF to evaluate the safety and efficacy of the drug.
After submitting a UNASYN 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 UNASYN API can apply through the Korea Drug Master File (KDMF).
click here to find a list of UNASYN suppliers with KDMF on PharmaCompass.
A UNASYN CEP of the European Pharmacopoeia monograph is often referred to as a UNASYN Certificate of Suitability (COS). The purpose of a UNASYN CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of UNASYN EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of UNASYN to their clients by showing that a UNASYN CEP has been issued for it. The manufacturer submits a UNASYN CEP (COS) as part of the market authorization procedure, and it takes on the role of a UNASYN CEP holder for the record. Additionally, the data presented in the UNASYN CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the UNASYN DMF.
A UNASYN CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. UNASYN 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 UNASYN suppliers with CEP (COS) on PharmaCompass.
A UNASYN written confirmation (UNASYN WC) is an official document issued by a regulatory agency to a UNASYN manufacturer, verifying that the manufacturing facility of a UNASYN active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting UNASYN APIs or UNASYN finished pharmaceutical products to another nation, regulatory agencies frequently require a UNASYN WC (written confirmation) as part of the regulatory process.
click here to find a list of UNASYN 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 UNASYN as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for UNASYN 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 UNASYN 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 UNASYN and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a UNASYN NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of UNASYN suppliers with NDC on PharmaCompass.
UNASYN 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 UNASYN 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 UNASYN GMP manufacturer or UNASYN GMP API supplier for your needs.
A UNASYN CoA (Certificate of Analysis) is a formal document that attests to UNASYN's compliance with UNASYN specifications and serves as a tool for batch-level quality control.
UNASYN CoA mostly includes findings from lab analyses of a specific batch. For each UNASYN 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.
UNASYN may be tested according to a variety of international standards, such as European Pharmacopoeia (UNASYN EP), UNASYN JP (Japanese Pharmacopeia) and the US Pharmacopoeia (UNASYN USP).
