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 E210 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E210, including repackagers and relabelers. The FDA regulates E210 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E210 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 E210 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E210 supplier is an individual or a company that provides E210 active pharmaceutical ingredient (API) or E210 finished formulations upon request. The E210 suppliers may include E210 API manufacturers, exporters, distributors and traders.
click here to find a list of E210 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 E210 Drug Master File in Japan (E210 JDMF) empowers E210 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 E210 JDMF during the approval evaluation for pharmaceutical products. At the time of E210 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 E210 suppliers with JDMF on PharmaCompass.
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