01 1ERREGIERRE S. p. A.
02 1Permakem Asia Co., Ltd.
01 2Nisoldipine
01 1Italy
02 1Japan
Registration Number : 217MF10589
Registrant's Address : VIA F. BARACCA 19-24060 SAN PAOLO D'ARGON (BERGAMO) ITALY
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2010-04-13
Registration Number : 217MF10719
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2010-02-12
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PharmaCompass offers a list of Nisoldipine 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 Nisoldipine manufacturer or Nisoldipine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nisoldipine manufacturer or Nisoldipine supplier.
PharmaCompass also assists you with knowing the Nisoldipine API Price utilized in the formulation of products. Nisoldipine API Price is not always fixed or binding as the Nisoldipine Price is obtained through a variety of data sources. The Nisoldipine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sular manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sular, including repackagers and relabelers. The FDA regulates Sular manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sular 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 Sular manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sular supplier is an individual or a company that provides Sular active pharmaceutical ingredient (API) or Sular finished formulations upon request. The Sular suppliers may include Sular API manufacturers, exporters, distributors and traders.
click here to find a list of Sular 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 Sular Drug Master File in Japan (Sular JDMF) empowers Sular 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 Sular JDMF during the approval evaluation for pharmaceutical products. At the time of Sular 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 Sular suppliers with JDMF on PharmaCompass.
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