01 1Zhejiang Ausun Pharmaceutical Co. , Ltd.
01 1Sitafloxacin hydrate
01 1China
Registration Number : 228MF10177
Registrant's Address : No. 5, Donghai 4th Avenue, Zhejiang Chemical Materials Base Linhai Zone, Zhejiang, Ch...
Initial Date of Registration : 2016-08-29
Latest Date of Registration : 2024-06-12
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PharmaCompass offers a list of Sitafloxacin Hydrate 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 Sitafloxacin Hydrate manufacturer or Sitafloxacin Hydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sitafloxacin Hydrate manufacturer or Sitafloxacin Hydrate supplier.
PharmaCompass also assists you with knowing the Sitafloxacin Hydrate API Price utilized in the formulation of products. Sitafloxacin Hydrate API Price is not always fixed or binding as the Sitafloxacin Hydrate Price is obtained through a variety of data sources. The Sitafloxacin Hydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gracevit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gracevit, including repackagers and relabelers. The FDA regulates Gracevit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gracevit 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 Gracevit manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gracevit supplier is an individual or a company that provides Gracevit active pharmaceutical ingredient (API) or Gracevit finished formulations upon request. The Gracevit suppliers may include Gracevit API manufacturers, exporters, distributors and traders.
click here to find a list of Gracevit 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 Gracevit Drug Master File in Japan (Gracevit JDMF) empowers Gracevit 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 Gracevit JDMF during the approval evaluation for pharmaceutical products. At the time of Gracevit 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 Gracevit suppliers with JDMF on PharmaCompass.
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