01 1Aurisco Pharmaceutical Co. , Ltd.
01 116α-hydroxyprednisolone
01 1China
Registration Number : 308MF10017
Registrant's Address : Badu Industrial Park Zone, Tiantai, Zhejiang province, 317200, P. R. China
Initial Date of Registration : 2026-01-21
Latest Date of Registration : 2026-01-21
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PharmaCompass offers a list of Desonide 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 Desonide manufacturer or Desonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Desonide manufacturer or Desonide supplier.
A Desonida manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desonida, including repackagers and relabelers. The FDA regulates Desonida manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desonida 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 Desonida manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Desonida supplier is an individual or a company that provides Desonida active pharmaceutical ingredient (API) or Desonida finished formulations upon request. The Desonida suppliers may include Desonida API manufacturers, exporters, distributors and traders.
click here to find a list of Desonida 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 Desonida Drug Master File in Japan (Desonida JDMF) empowers Desonida 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 Desonida JDMF during the approval evaluation for pharmaceutical products. At the time of Desonida 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 Desonida suppliers with JDMF on PharmaCompass.
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