01 1Cambrex Profarmaco Milano S. r. l.
02 1Shizuoka Caffeine Industry Co., Ltd.
01 1Bisacodyl
02 1Japanese Pharmacopoeia bisacodyl (production only)
01 1Japan
02 1U.S.A
Registration Number : 218MF10142
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2015-08-18
Japanese Pharmacopoeia Bisacodyl (for manufacturing only)
Registration Number : 217MF10614
Registrant's Address : 129 Suidocho, Aoi Ward, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2008-02-25
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PharmaCompass offers a list of Bisacodyl 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 Bisacodyl manufacturer or Bisacodyl supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bisacodyl manufacturer or Bisacodyl supplier.
PharmaCompass also assists you with knowing the Bisacodyl API Price utilized in the formulation of products. Bisacodyl API Price is not always fixed or binding as the Bisacodyl Price is obtained through a variety of data sources. The Bisacodyl Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LS-2218 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LS-2218, including repackagers and relabelers. The FDA regulates LS-2218 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LS-2218 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 LS-2218 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LS-2218 supplier is an individual or a company that provides LS-2218 active pharmaceutical ingredient (API) or LS-2218 finished formulations upon request. The LS-2218 suppliers may include LS-2218 API manufacturers, exporters, distributors and traders.
click here to find a list of LS-2218 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 LS-2218 Drug Master File in Japan (LS-2218 JDMF) empowers LS-2218 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 LS-2218 JDMF during the approval evaluation for pharmaceutical products. At the time of LS-2218 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 LS-2218 suppliers with JDMF on PharmaCompass.
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