01 1SperaNexus Inc.
01 1Hydrochloric acid delapril
01 1Japan
Registration Number : 217MF10055
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2009-03-16
79
PharmaCompass offers a list of Delapril 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 Delapril Hydrochloride manufacturer or Delapril Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Delapril Hydrochloride manufacturer or Delapril Hydrochloride supplier.
PharmaCompass also assists you with knowing the Delapril Hydrochloride API Price utilized in the formulation of products. Delapril Hydrochloride API Price is not always fixed or binding as the Delapril Hydrochloride Price is obtained through a variety of data sources. The Delapril Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A derapril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of derapril, including repackagers and relabelers. The FDA regulates derapril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. derapril 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 derapril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A derapril supplier is an individual or a company that provides derapril active pharmaceutical ingredient (API) or derapril finished formulations upon request. The derapril suppliers may include derapril API manufacturers, exporters, distributors and traders.
click here to find a list of derapril 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 derapril Drug Master File in Japan (derapril JDMF) empowers derapril 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 derapril JDMF during the approval evaluation for pharmaceutical products. At the time of derapril 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 derapril suppliers with JDMF on PharmaCompass.
We have 1 companies offering derapril
Get in contact with the supplier of your choice:
