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1. Hmbromide
2. Homatropine Methylbromide
3. Homatropine Methylbromide Iodide, (3(r)-endo)-isomer
4. Homatropine Methylbromide Iodide, (3(s)-endo)-isomer
5. Homatropine Methylbromide, (3(r)-endo)-isomer
6. Homatropine Methylbromide, (3(s)-endo)-isomer
7. Homatropine Methylbromide, Endo-(+-)-isomer
1. Homatropine Methylbromide
2. Homatropine Methobromide
3. Omatropina Metilbromuro
4. Methylhomatropine Bromide
5. 80-49-9
6. 8-methylhomatropinium Bromide
7. Tropinium Methobromide Mandelate
8. Homatropine Methyl Bromide
9. Methylhomatropinum Bromatum
10. Methylbromure D'homatropine
11. 3-alpha-hydroxy-8-methyl-1-alpha-h,5-alpha-h-tropanium Bromide Mandelate
12. Nsc34399
13. Schembl77827
14. Chebi:50373
15. Akos015896228
16. Db00725
17. 3-[2-hydroxy(phenyl)acetoxy]-8,8-dimethyl-8-azoniabicyclo[3.2.1]octane Bromide
18. Ncgc00094694-01
19. Ncgc00094694-02
20. Db-056442
21. D90875
22. H-2560
Molecular Weight | 370.3 g/mol |
---|---|
Molecular Formula | C17H24BrNO3 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 4 |
Exact Mass | 369.09396 g/mol |
Monoisotopic Mass | 369.09396 g/mol |
Topological Polar Surface Area | 46.5 Ų |
Heavy Atom Count | 22 |
Formal Charge | 0 |
Complexity | 374 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 3 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
Used in conjunction with antacids or histamine H2-receptor antagonists in the treatment of peptic ulcers, gastric ulcers and duodenal ulcers, to reduce further gastric acid secretion and delay gastric emptying.
Homatropine methylbromide belongs to the group of medicines called anti-muscarinics. Homatropine is used to treat duodenal or stomach ulcers or intestine problems. It can be used together with antacids or other medicine in the treatment of peptic ulcer. It may also be used to prevent nausea, vomiting, and motion sickness.
A - Alimentary tract and metabolism
A03 - Drugs for functional gastrointestinal disorders
A03B - Belladonna and derivatives, plain
A03BB - Belladonna alkaloids, semisynthetic, quaternary ammonium compounds
A03BB06 - Homatropine methylbromide
Homatropine is a quaternary ammonium muscarinic acetylcholine receptor antagonist. The muscarinic acetylcholine receptor mediates various cellular responses, including inhibition of adenylate cyclase, breakdown of phosphoinositides and modulation of potassium channels through the action of G proteins. Homatropine methylbromide inhibits the muscarinic actions of acetylcholine on structures innervated by postganglionic cholinergic nerves as well as on smooth muscles that respond to acetylcholine but lack cholinergic innervation. These postganglionic receptor sites are present in the autonomic effector cells of the smooth muscle, cardiac muscle, sinoatrial and atrioventricular nodes, and exocrine glands. Depending on the dose, anticholinergics may reduce the motility and secretory activity of the gastrointestinal system, and the tone of the ureter and urinary bladder and may have a slight relaxant action on the bile ducts and gallbladder.
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PharmaCompass offers a list of Homatropine Methylbromide 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 Homatropine Methylbromide manufacturer or Homatropine Methylbromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Homatropine Methylbromide manufacturer or Homatropine Methylbromide supplier.
PharmaCompass also assists you with knowing the Homatropine Methylbromide API Price utilized in the formulation of products. Homatropine Methylbromide API Price is not always fixed or binding as the Homatropine Methylbromide Price is obtained through a variety of data sources. The Homatropine Methylbromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Metilbromuro de homatropina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metilbromuro de homatropina, including repackagers and relabelers. The FDA regulates Metilbromuro de homatropina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metilbromuro de homatropina 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 Metilbromuro de homatropina supplier is an individual or a company that provides Metilbromuro de homatropina active pharmaceutical ingredient (API) or Metilbromuro de homatropina finished formulations upon request. The Metilbromuro de homatropina suppliers may include Metilbromuro de homatropina API manufacturers, exporters, distributors and traders.
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A Metilbromuro de homatropina DMF (Drug Master File) is a document detailing the whole manufacturing process of Metilbromuro de homatropina active pharmaceutical ingredient (API) in detail. Different forms of Metilbromuro de homatropina DMFs exist exist since differing nations have different regulations, such as Metilbromuro de homatropina USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Metilbromuro de homatropina DMF submitted to regulatory agencies in the US is known as a USDMF. Metilbromuro de homatropina USDMF includes data on Metilbromuro de homatropina's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Metilbromuro de homatropina USDMF is kept confidential to protect the manufacturer’s intellectual property.
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A Metilbromuro de homatropina CEP of the European Pharmacopoeia monograph is often referred to as a Metilbromuro de homatropina Certificate of Suitability (COS). The purpose of a Metilbromuro de homatropina CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Metilbromuro de homatropina EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Metilbromuro de homatropina to their clients by showing that a Metilbromuro de homatropina CEP has been issued for it. The manufacturer submits a Metilbromuro de homatropina CEP (COS) as part of the market authorization procedure, and it takes on the role of a Metilbromuro de homatropina CEP holder for the record. Additionally, the data presented in the Metilbromuro de homatropina CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Metilbromuro de homatropina DMF.
A Metilbromuro de homatropina CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Metilbromuro de homatropina 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 Metilbromuro de homatropina written confirmation (Metilbromuro de homatropina WC) is an official document issued by a regulatory agency to a Metilbromuro de homatropina manufacturer, verifying that the manufacturing facility of a Metilbromuro de homatropina active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Metilbromuro de homatropina APIs or Metilbromuro de homatropina finished pharmaceutical products to another nation, regulatory agencies frequently require a Metilbromuro de homatropina 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 Metilbromuro de homatropina as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Metilbromuro de homatropina 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 Metilbromuro de homatropina 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 Metilbromuro de homatropina and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Metilbromuro de homatropina NDC to their finished compounded human drug products, they may choose to do so.
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Metilbromuro de homatropina 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 Metilbromuro de homatropina 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 Metilbromuro de homatropina GMP manufacturer or Metilbromuro de homatropina GMP API supplier for your needs.
A Metilbromuro de homatropina CoA (Certificate of Analysis) is a formal document that attests to Metilbromuro de homatropina's compliance with Metilbromuro de homatropina specifications and serves as a tool for batch-level quality control.
Metilbromuro de homatropina CoA mostly includes findings from lab analyses of a specific batch. For each Metilbromuro de homatropina 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.
Metilbromuro de homatropina may be tested according to a variety of international standards, such as European Pharmacopoeia (Metilbromuro de homatropina EP), Metilbromuro de homatropina JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Metilbromuro de homatropina USP).