01 1Kyorin Pharmaceutical Group Factory Co., Ltd.
01 1Gatifloxacin
01 1Japan
Registration Number : 218MF10335
Registrant's Address : 6 Kanda Surugadai 4-chome, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2009-07-09
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PharmaCompass offers a list of Gatifloxacin 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 Gatifloxacin manufacturer or Gatifloxacin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gatifloxacin manufacturer or Gatifloxacin supplier.
PharmaCompass also assists you with knowing the Gatifloxacin API Price utilized in the formulation of products. Gatifloxacin API Price is not always fixed or binding as the Gatifloxacin Price is obtained through a variety of data sources. The Gatifloxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zymaxid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zymaxid, including repackagers and relabelers. The FDA regulates Zymaxid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zymaxid 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 Zymaxid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zymaxid supplier is an individual or a company that provides Zymaxid active pharmaceutical ingredient (API) or Zymaxid finished formulations upon request. The Zymaxid suppliers may include Zymaxid API manufacturers, exporters, distributors and traders.
click here to find a list of Zymaxid 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 Zymaxid Drug Master File in Japan (Zymaxid JDMF) empowers Zymaxid 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 Zymaxid JDMF during the approval evaluation for pharmaceutical products. At the time of Zymaxid 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 Zymaxid suppliers with JDMF on PharmaCompass.
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