01 1Sogo Pharmaceutical Co., Ltd.
01 1Chlorhexidine hydrochloride
01 1U.S.A
Registration Number : 217MF10423
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-08-19
Latest Date of Registration : 2021-07-20
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PharmaCompass offers a list of Chlorhexidine HCl 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 Chlorhexidine HCl manufacturer or Chlorhexidine HCl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorhexidine HCl manufacturer or Chlorhexidine HCl supplier.
PharmaCompass also assists you with knowing the Chlorhexidine HCl API Price utilized in the formulation of products. Chlorhexidine HCl API Price is not always fixed or binding as the Chlorhexidine HCl Price is obtained through a variety of data sources. The Chlorhexidine HCl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Chlorhexidine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorhexidine Dihydrochloride, including repackagers and relabelers. The FDA regulates Chlorhexidine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorhexidine Dihydrochloride 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 Chlorhexidine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorhexidine Dihydrochloride supplier is an individual or a company that provides Chlorhexidine Dihydrochloride active pharmaceutical ingredient (API) or Chlorhexidine Dihydrochloride finished formulations upon request. The Chlorhexidine Dihydrochloride suppliers may include Chlorhexidine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorhexidine Dihydrochloride 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 Chlorhexidine Dihydrochloride Drug Master File in Japan (Chlorhexidine Dihydrochloride JDMF) empowers Chlorhexidine Dihydrochloride 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 Chlorhexidine Dihydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorhexidine Dihydrochloride 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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