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 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 Chlorhexidine Hydrochloride manufacturer or Chlorhexidine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorhexidine Hydrochloride manufacturer or Chlorhexidine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Chlorhexidine Hydrochloride API Price utilized in the formulation of products. Chlorhexidine Hydrochloride API Price is not always fixed or binding as the Chlorhexidine Hydrochloride Price is obtained through a variety of data sources. The Chlorhexidine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dantroche hibitane manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dantroche hibitane, including repackagers and relabelers. The FDA regulates Dantroche hibitane manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dantroche hibitane 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 Dantroche hibitane supplier is an individual or a company that provides Dantroche hibitane active pharmaceutical ingredient (API) or Dantroche hibitane finished formulations upon request. The Dantroche hibitane suppliers may include Dantroche hibitane API manufacturers, exporters, distributors and traders.
click here to find a list of Dantroche hibitane 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 Dantroche hibitane Drug Master File in Japan (Dantroche hibitane JDMF) empowers Dantroche hibitane 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 Dantroche hibitane JDMF during the approval evaluation for pharmaceutical products. At the time of Dantroche hibitane 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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