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1. Bi-citrate
2. Biselic
3. Bismofarma
4. Bismuth Citrate
5. Bismuth Tripotassium Dicitrate
6. Colloidal Bismuth Subcitrate
7. De-nol
8. De-noltab
9. Denol
10. Gastrodenol
11. Sucrato
12. Tripotassium-dicitrato Bismuthate
13. Ventrisol-polfa
1. Gastrodenol
2. Bismuth Tripotassium Dicitrate
3. 57644-54-9
4. Colloidal Bismuth Subcitrate
5. Tripotassium Dicitratobismuthate
6. Hs813p8qpx
7. Bismuth;tripotassium;2-hydroxypropane-1,2,3-tricarboxylate
8. Bismuth Subcitrate Potassium
9. De-noltab
10. 1,2,3-propanetricarboxylic Acid, 2-hydroxy-, Bismuth(3+) Potassium Salt (2:1:3)
11. Tripotassium;2-hydroxypropane-1,2,3-tricarboxylate;5-hydroxy-2,8,9-trioxa-1-bismabicyclo[3.3.2]decane-3,7,10-trione
12. Unii-hs813p8qpx
13. Einecs 260-872-5
14. De-nol (tn)
15. Tripotassium Dicitrate Bismuthate
16. Bismuth Subcitrate [vandf]
17. Bcp10508
18. Bismuth Subcitrate [who-dd]
19. Hy-b0796
20. Bismuth Subcitrate, Colloidal
21. Mfcd02101411
22. Akos005110988
23. Cs-3966
24. Colloidal Bismuth Subcitrate [mi]
25. B4377
26. Ft-0623129
27. D07587
28. Tripotassium Dicitratobismuthate [who-dd]
29. Bismuth(iii) Tripotassium 2-hydroxypropane-1,2,3-tricarboxylate
30. Bismuth(3+) Tripotassium Bis(2-hydroxypropane-1,2,3-tricarboxylate)
31. Bismuth Tripotassium Dicitrate; Bismuth Subcitrate; Duosol; Gastrodenol; Bismuth Subcitrate Potassium; De-nol
Molecular Weight | 704.47 g/mol |
---|---|
Molecular Formula | C12H10BiK3O14 |
Hydrogen Bond Donor Count | 2 |
Hydrogen Bond Acceptor Count | 14 |
Rotatable Bond Count | 4 |
Exact Mass | 703.87857 g/mol |
Monoisotopic Mass | 703.87857 g/mol |
Topological Polar Surface Area | 281 Ų |
Heavy Atom Count | 30 |
Formal Charge | 0 |
Complexity | 211 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 6 |
Antacids
Substances that counteract or neutralize acidity of the GASTROINTESTINAL TRACT. (See all compounds classified as Antacids.)
Anti-Infective Agents
Substances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection. (See all compounds classified as Anti-Infective Agents.)
Anti-Ulcer Agents
Various agents with different action mechanisms used to treat or ameliorate PEPTIC ULCER or irritation of the gastrointestinal tract. This has included ANTIBIOTICS to treat HELICOBACTER INFECTIONS; HISTAMINE H2 ANTAGONISTS to reduce GASTRIC ACID secretion; and ANTACIDS for symptomatic relief. (See all compounds classified as Anti-Ulcer Agents.)
A - Alimentary tract and metabolism
A02 - Drugs for acid related disorders
A02B - Drugs for peptic ulcer and gastro-oesophageal reflux disease (gord)
A02BX - Other drugs for peptic ulcer and gastro-oesophageal reflux disease (gord)
A02BX05 - Bismuth subcitrate
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PharmaCompass offers a list of Bismuth Potassium Citrate 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 Bismuth Potassium Citrate manufacturer or Bismuth Potassium Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bismuth Potassium Citrate manufacturer or Bismuth Potassium Citrate supplier.
PharmaCompass also assists you with knowing the Bismuth Potassium Citrate API Price utilized in the formulation of products. Bismuth Potassium Citrate API Price is not always fixed or binding as the Bismuth Potassium Citrate Price is obtained through a variety of data sources. The Bismuth Potassium Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A bismuth tripotassium dicitrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of bismuth tripotassium dicitrate, including repackagers and relabelers. The FDA regulates bismuth tripotassium dicitrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. bismuth tripotassium dicitrate 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 bismuth tripotassium dicitrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A bismuth tripotassium dicitrate supplier is an individual or a company that provides bismuth tripotassium dicitrate active pharmaceutical ingredient (API) or bismuth tripotassium dicitrate finished formulations upon request. The bismuth tripotassium dicitrate suppliers may include bismuth tripotassium dicitrate API manufacturers, exporters, distributors and traders.
click here to find a list of bismuth tripotassium dicitrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A bismuth tripotassium dicitrate DMF (Drug Master File) is a document detailing the whole manufacturing process of bismuth tripotassium dicitrate active pharmaceutical ingredient (API) in detail. Different forms of bismuth tripotassium dicitrate DMFs exist exist since differing nations have different regulations, such as bismuth tripotassium dicitrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A bismuth tripotassium dicitrate DMF submitted to regulatory agencies in the US is known as a USDMF. bismuth tripotassium dicitrate USDMF includes data on bismuth tripotassium dicitrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The bismuth tripotassium dicitrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of bismuth tripotassium dicitrate suppliers with USDMF 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 bismuth tripotassium dicitrate Drug Master File in Korea (bismuth tripotassium dicitrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of bismuth tripotassium dicitrate. The MFDS reviews the bismuth tripotassium dicitrate KDMF as part of the drug registration process and uses the information provided in the bismuth tripotassium dicitrate KDMF to evaluate the safety and efficacy of the drug.
After submitting a bismuth tripotassium dicitrate 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 bismuth tripotassium dicitrate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of bismuth tripotassium dicitrate suppliers with KDMF on PharmaCompass.
bismuth tripotassium dicitrate 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 bismuth tripotassium dicitrate 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 bismuth tripotassium dicitrate GMP manufacturer or bismuth tripotassium dicitrate GMP API supplier for your needs.
A bismuth tripotassium dicitrate CoA (Certificate of Analysis) is a formal document that attests to bismuth tripotassium dicitrate's compliance with bismuth tripotassium dicitrate specifications and serves as a tool for batch-level quality control.
bismuth tripotassium dicitrate CoA mostly includes findings from lab analyses of a specific batch. For each bismuth tripotassium dicitrate 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.
bismuth tripotassium dicitrate may be tested according to a variety of international standards, such as European Pharmacopoeia (bismuth tripotassium dicitrate EP), bismuth tripotassium dicitrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (bismuth tripotassium dicitrate USP).