01 1Ishihara Sangyo Kaisha, Ltd.
01 1Cevimeline (ISK)
01 1Japan
Cevimeline hydrochloride (ISK)
Registration Number : 218MF10409
Registrant's Address : 1-3-15 Edobori, Nishi-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2006-04-14
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PharmaCompass offers a list of Cevimeline 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 Cevimeline Hydrochloride manufacturer or Cevimeline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cevimeline Hydrochloride manufacturer or Cevimeline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cevimeline Hydrochloride API Price utilized in the formulation of products. Cevimeline Hydrochloride API Price is not always fixed or binding as the Cevimeline Hydrochloride Price is obtained through a variety of data sources. The Cevimeline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cevimeline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cevimeline Hydrochloride, including repackagers and relabelers. The FDA regulates Cevimeline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cevimeline Hydrochloride 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 Cevimeline Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cevimeline Hydrochloride supplier is an individual or a company that provides Cevimeline Hydrochloride active pharmaceutical ingredient (API) or Cevimeline Hydrochloride finished formulations upon request. The Cevimeline Hydrochloride suppliers may include Cevimeline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cevimeline Hydrochloride 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 Cevimeline Hydrochloride Drug Master File in Japan (Cevimeline Hydrochloride JDMF) empowers Cevimeline Hydrochloride 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 Cevimeline Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Cevimeline Hydrochloride 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 Cevimeline Hydrochloride suppliers with JDMF on PharmaCompass.
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