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1. 2-(diethylaminoethyl)thioacetoxymutilin
2. 81723 Hfu
3. Dynamutilin
4. Tiamulin
5. Tiamulin Fumarate
6. Tiamulin Fumarate (1:1), (3as-(3aalpha,4beta,5alpha,6alpha,8beta,9alpha,9abeta,10s*))-isomer
7. Tiamulin Hydrochloride
8. Tiamutin
1. Tiamulin Fumarate
2. 55297-96-6
3. Dtxsid901020751
4. Akos015896409
| Molecular Weight | 609.8 g/mol |
|---|---|
| Molecular Formula | C32H51NO8S |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 12 |
| Exact Mass | 609.33353876 g/mol |
| Monoisotopic Mass | 609.33353876 g/mol |
| Topological Polar Surface Area | 167 Ų |
| Heavy Atom Count | 42 |
| Formal Charge | 0 |
| Complexity | 889 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 6 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently Bonded Unit Count | 2 |
Anti-Bacterial Agents
Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)
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ABOUT THIS PAGE
A Tiamulin Hydrogen Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiamulin Hydrogen Fumarate, including repackagers and relabelers. The FDA regulates Tiamulin Hydrogen Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiamulin Hydrogen Fumarate 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 Tiamulin Hydrogen Fumarate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tiamulin Hydrogen Fumarate supplier is an individual or a company that provides Tiamulin Hydrogen Fumarate active pharmaceutical ingredient (API) or Tiamulin Hydrogen Fumarate finished formulations upon request. The Tiamulin Hydrogen Fumarate suppliers may include Tiamulin Hydrogen Fumarate API manufacturers, exporters, distributors and traders.
click here to find a list of Tiamulin Hydrogen Fumarate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tiamulin Hydrogen Fumarate DMF (Drug Master File) is a document detailing the whole manufacturing process of Tiamulin Hydrogen Fumarate active pharmaceutical ingredient (API) in detail. Different forms of Tiamulin Hydrogen Fumarate DMFs exist exist since differing nations have different regulations, such as Tiamulin Hydrogen Fumarate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tiamulin Hydrogen Fumarate DMF submitted to regulatory agencies in the US is known as a USDMF. Tiamulin Hydrogen Fumarate USDMF includes data on Tiamulin Hydrogen Fumarate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tiamulin Hydrogen Fumarate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Tiamulin Hydrogen Fumarate suppliers with USDMF on PharmaCompass.
A Tiamulin Hydrogen Fumarate CEP of the European Pharmacopoeia monograph is often referred to as a Tiamulin Hydrogen Fumarate Certificate of Suitability (COS). The purpose of a Tiamulin Hydrogen Fumarate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tiamulin Hydrogen Fumarate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tiamulin Hydrogen Fumarate to their clients by showing that a Tiamulin Hydrogen Fumarate CEP has been issued for it. The manufacturer submits a Tiamulin Hydrogen Fumarate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tiamulin Hydrogen Fumarate CEP holder for the record. Additionally, the data presented in the Tiamulin Hydrogen Fumarate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tiamulin Hydrogen Fumarate DMF.
A Tiamulin Hydrogen Fumarate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tiamulin Hydrogen Fumarate 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 Tiamulin Hydrogen Fumarate suppliers with CEP (COS) 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 Tiamulin Hydrogen Fumarate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tiamulin Hydrogen Fumarate 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 Tiamulin Hydrogen Fumarate 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 Tiamulin Hydrogen Fumarate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tiamulin Hydrogen Fumarate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tiamulin Hydrogen Fumarate suppliers with NDC on PharmaCompass.
Tiamulin Hydrogen Fumarate 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 Tiamulin Hydrogen Fumarate 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 Tiamulin Hydrogen Fumarate GMP manufacturer or Tiamulin Hydrogen Fumarate GMP API supplier for your needs.
A Tiamulin Hydrogen Fumarate CoA (Certificate of Analysis) is a formal document that attests to Tiamulin Hydrogen Fumarate's compliance with Tiamulin Hydrogen Fumarate specifications and serves as a tool for batch-level quality control.
Tiamulin Hydrogen Fumarate CoA mostly includes findings from lab analyses of a specific batch. For each Tiamulin Hydrogen Fumarate 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.
Tiamulin Hydrogen Fumarate may be tested according to a variety of international standards, such as European Pharmacopoeia (Tiamulin Hydrogen Fumarate EP), Tiamulin Hydrogen Fumarate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Tiamulin Hydrogen Fumarate USP).
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