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1. 123333-71-1
2. Dl-histidine Monohydrochloride Monohydrate
3. 2-amino-3-(1h-imidazol-4-yl)propanoic Acid Hydrochloride Hydrate
4. 2-amino-3-(1h-imidazol-5-yl)propanoic Acid;hydrate;hydrochloride
5. Dl-histidine Hydrochloride 1-hydrate
6. L-histidine Hcl Monohydrate
7. Histidine, Chloride, Hydrate
8. Mfcd00151028
9. D,l-his.hcl.h2o
10. Schembl50269
11. Ccris 7814
12. D-histidine Hydrochloride Hydrate
13. Dtxsid10924465
14. Dl-histidine Hydrochloride Hydrate
15. L-histidine, Hydrochloride, Hydrate
16. Dl-histidine Hydrochloride Monohydrate
17. Akos016890704
18. Cs-w015138
19. Dl-histidinemonohydrochloridemonohydrate
20. As-14792
21. Db-041722
22. Dl-histidine, Monohydrochloride, Monohydrate
23. Ft-0627600
24. Ft-0643003
25. A805051
26. Dl-histidine Monohydrochloride Monohydrate, >=99% (tlc)
Molecular Weight | 209.63 g/mol |
---|---|
Molecular Formula | C6H12ClN3O3 |
Hydrogen Bond Donor Count | 5 |
Hydrogen Bond Acceptor Count | 5 |
Rotatable Bond Count | 3 |
Exact Mass | 209.0567189 g/mol |
Monoisotopic Mass | 209.0567189 g/mol |
Topological Polar Surface Area | 93 Ų |
Heavy Atom Count | 13 |
Formal Charge | 0 |
Complexity | 151 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 1 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 3 |
Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Dl-Histidine Monohydrochloride Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dl-Histidine Monohydrochloride Monohydrate, including repackagers and relabelers. The FDA regulates Dl-Histidine Monohydrochloride Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dl-Histidine Monohydrochloride Monohydrate 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 Dl-Histidine Monohydrochloride Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dl-Histidine Monohydrochloride Monohydrate supplier is an individual or a company that provides Dl-Histidine Monohydrochloride Monohydrate active pharmaceutical ingredient (API) or Dl-Histidine Monohydrochloride Monohydrate finished formulations upon request. The Dl-Histidine Monohydrochloride Monohydrate suppliers may include Dl-Histidine Monohydrochloride Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Dl-Histidine Monohydrochloride Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dl-Histidine Monohydrochloride Monohydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Dl-Histidine Monohydrochloride Monohydrate active pharmaceutical ingredient (API) in detail. Different forms of Dl-Histidine Monohydrochloride Monohydrate DMFs exist exist since differing nations have different regulations, such as Dl-Histidine Monohydrochloride Monohydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dl-Histidine Monohydrochloride Monohydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Dl-Histidine Monohydrochloride Monohydrate USDMF includes data on Dl-Histidine Monohydrochloride Monohydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dl-Histidine Monohydrochloride Monohydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dl-Histidine Monohydrochloride Monohydrate 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 Dl-Histidine Monohydrochloride Monohydrate Drug Master File in Japan (Dl-Histidine Monohydrochloride Monohydrate JDMF) empowers Dl-Histidine Monohydrochloride Monohydrate 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 Dl-Histidine Monohydrochloride Monohydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Dl-Histidine Monohydrochloride Monohydrate 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 Dl-Histidine Monohydrochloride Monohydrate suppliers with JDMF on PharmaCompass.
Dl-Histidine Monohydrochloride Monohydrate 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 Dl-Histidine Monohydrochloride Monohydrate 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 Dl-Histidine Monohydrochloride Monohydrate GMP manufacturer or Dl-Histidine Monohydrochloride Monohydrate GMP API supplier for your needs.
A Dl-Histidine Monohydrochloride Monohydrate CoA (Certificate of Analysis) is a formal document that attests to Dl-Histidine Monohydrochloride Monohydrate's compliance with Dl-Histidine Monohydrochloride Monohydrate specifications and serves as a tool for batch-level quality control.
Dl-Histidine Monohydrochloride Monohydrate CoA mostly includes findings from lab analyses of a specific batch. For each Dl-Histidine Monohydrochloride Monohydrate 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.
Dl-Histidine Monohydrochloride Monohydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Dl-Histidine Monohydrochloride Monohydrate EP), Dl-Histidine Monohydrochloride Monohydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dl-Histidine Monohydrochloride Monohydrate USP).
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