01 1Kongo Chemical Co., Ltd.
01 1Diphenhydramine hydrochloride (production only)
01 1Japan
Diphenhydramine hydrochloride (for manufacturing purposes only)
Registration Number : 217MF11188
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-03-09
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PharmaCompass offers a list of Diphenhydramine Hydrochloride 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 Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Diphenhydramine Hydrochloride API Price utilized in the formulation of products. Diphenhydramine Hydrochloride API Price is not always fixed or binding as the Diphenhydramine Hydrochloride Price is obtained through a variety of data sources. The Diphenhydramine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride, including repackagers and relabelers. The FDA regulates 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride 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 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride supplier is an individual or a company that provides 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride active pharmaceutical ingredient (API) or 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride finished formulations upon request. The 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride suppliers may include 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride 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 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride Drug Master File in Japan (2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride JDMF) empowers 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride 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 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of 2-(diphenylmethoxy)-N,N-dimethylethanamine h ydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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