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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diphenhydramine Hydrochloride manufacturer or Diphenhydramine Hydrochloride supplier.
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 DIPHENHYDRAMINE HCL 100MG S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIPHENHYDRAMINE HCL 100MG S, including repackagers and relabelers. The FDA regulates DIPHENHYDRAMINE HCL 100MG S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIPHENHYDRAMINE HCL 100MG S 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 DIPHENHYDRAMINE HCL 100MG S supplier is an individual or a company that provides DIPHENHYDRAMINE HCL 100MG S active pharmaceutical ingredient (API) or DIPHENHYDRAMINE HCL 100MG S finished formulations upon request. The DIPHENHYDRAMINE HCL 100MG S suppliers may include DIPHENHYDRAMINE HCL 100MG S API manufacturers, exporters, distributors and traders.
click here to find a list of DIPHENHYDRAMINE HCL 100MG S 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 DIPHENHYDRAMINE HCL 100MG S Drug Master File in Japan (DIPHENHYDRAMINE HCL 100MG S JDMF) empowers DIPHENHYDRAMINE HCL 100MG S 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 DIPHENHYDRAMINE HCL 100MG S JDMF during the approval evaluation for pharmaceutical products. At the time of DIPHENHYDRAMINE HCL 100MG S 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 DIPHENHYDRAMINE HCL 100MG S suppliers with JDMF on PharmaCompass.
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