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1. Homochlorcyclizine Hcl
2. 24342-55-0
3. 1-[(4-chlorophenyl)-phenylmethyl]-4-methyl-1,4-diazepan-4-ium;chloride
4. Homochlorcyclizine Hydrochloride [jan]
5. 1-(p-chloro-alpha-phenylbenzyl)hexahydro-4-methyl-1h-1,4-diazepine Hydrochloride
6. 1h-1,4-diazepine, 1-((4-chlorophenyl)phenylmethyl)hexahydro-4-methyl-, Hydrochloride
7. 1h-1,4-diazepine, 1-(p-chloro-alpha-phenylbenzyl)hexahydro-4-methyl-, Hydrochloride
| Molecular Weight | 351.3 g/mol |
|---|---|
| Molecular Formula | C19H24Cl2N2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 350.1316542 g/mol |
| Monoisotopic Mass | 350.1316542 g/mol |
| Topological Polar Surface Area | 7.7 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 321 |
| 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 | 2 |
ABOUT THIS PAGE
A Homochlorcyclizine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Homochlorcyclizine Hydrochloride, including repackagers and relabelers. The FDA regulates Homochlorcyclizine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Homochlorcyclizine Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Homochlorcyclizine Hydrochloride supplier is an individual or a company that provides Homochlorcyclizine Hydrochloride active pharmaceutical ingredient (API) or Homochlorcyclizine Hydrochloride finished formulations upon request. The Homochlorcyclizine Hydrochloride suppliers may include Homochlorcyclizine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Homochlorcyclizine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Homochlorcyclizine Hydrochloride Drug Master File in Japan (Homochlorcyclizine Hydrochloride JDMF) empowers Homochlorcyclizine Hydrochloride 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 Homochlorcyclizine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Homochlorcyclizine Hydrochloride 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 Homochlorcyclizine Hydrochloride suppliers with JDMF on PharmaCompass.
Homochlorcyclizine Hydrochloride 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 Homochlorcyclizine Hydrochloride 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 Homochlorcyclizine Hydrochloride GMP manufacturer or Homochlorcyclizine Hydrochloride GMP API supplier for your needs.
A Homochlorcyclizine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Homochlorcyclizine Hydrochloride's compliance with Homochlorcyclizine Hydrochloride specifications and serves as a tool for batch-level quality control.
Homochlorcyclizine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Homochlorcyclizine Hydrochloride 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.
Homochlorcyclizine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Homochlorcyclizine Hydrochloride EP), Homochlorcyclizine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Homochlorcyclizine Hydrochloride USP).
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