01 2Kongo Chemical Co., Ltd.
01 1Diphenhydramine (production only)
02 1Salicylic acid diphenhydramine (production only)
01 2Japan
Diphenhydramine (for manufacturing purposes only)
Registration Number : 217MF11191
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2021-04-13
Diphenhydramine salicylate (for manufacturing purposes only)
Registration Number : 217MF11205
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 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 manufacturer or Diphenhydramine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diphenhydramine manufacturer or Diphenhydramine supplier.
PharmaCompass also assists you with knowing the Diphenhydramine API Price utilized in the formulation of products. Diphenhydramine API Price is not always fixed or binding as the Diphenhydramine Price is obtained through a variety of data sources. The Diphenhydramine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Difenidramina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Difenidramina, including repackagers and relabelers. The FDA regulates Difenidramina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Difenidramina 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 Difenidramina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Difenidramina supplier is an individual or a company that provides Difenidramina active pharmaceutical ingredient (API) or Difenidramina finished formulations upon request. The Difenidramina suppliers may include Difenidramina API manufacturers, exporters, distributors and traders.
click here to find a list of Difenidramina 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 Difenidramina Drug Master File in Japan (Difenidramina JDMF) empowers Difenidramina 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 Difenidramina JDMF during the approval evaluation for pharmaceutical products. At the time of Difenidramina 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 Difenidramina suppliers with JDMF on PharmaCompass.
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