01 1Sumitomo Chemical Co., Ltd.
01 1Japanese Pharmacopoeia mequitazine
01 1Japan
Japanese Pharmacopoeia Mequitazine
Registration Number : 218MF10270
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2006-02-17
Latest Date of Registration : 2007-04-27
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PharmaCompass offers a list of Mequitazine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Mequitazine manufacturer or Mequitazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mequitazine manufacturer or Mequitazine supplier.
A Zesulan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zesulan, including repackagers and relabelers. The FDA regulates Zesulan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zesulan 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 Zesulan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Zesulan supplier is an individual or a company that provides Zesulan active pharmaceutical ingredient (API) or Zesulan finished formulations upon request. The Zesulan suppliers may include Zesulan API manufacturers, exporters, distributors and traders.
click here to find a list of Zesulan suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Zesulan Drug Master File in Japan (Zesulan JDMF) empowers Zesulan 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 Zesulan JDMF during the approval evaluation for pharmaceutical products. At the time of Zesulan 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 Zesulan suppliers with JDMF on PharmaCompass.
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