01 1Active Pharma Inc.
01 1Piperidinoethoxy acetylamino benzoic acid ethyl
01 1Japan
Ethyl piperidinoacetylaminobenzoate
Registration Number : 227MF10187
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2015-07-23
Latest Date of Registration : 2021-05-10
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PharmaCompass offers a list of Benzoic Acid 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 Benzoic Acid manufacturer or Benzoic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benzoic Acid manufacturer or Benzoic Acid supplier.
PharmaCompass also assists you with knowing the Benzoic Acid API Price utilized in the formulation of products. Benzoic Acid API Price is not always fixed or binding as the Benzoic Acid Price is obtained through a variety of data sources. The Benzoic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BOX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BOX, including repackagers and relabelers. The FDA regulates BOX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BOX 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 BOX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BOX supplier is an individual or a company that provides BOX active pharmaceutical ingredient (API) or BOX finished formulations upon request. The BOX suppliers may include BOX API manufacturers, exporters, distributors and traders.
click here to find a list of BOX 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 BOX Drug Master File in Japan (BOX JDMF) empowers BOX 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 BOX JDMF during the approval evaluation for pharmaceutical products. At the time of BOX 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 BOX suppliers with JDMF on PharmaCompass.
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