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