01 1Sogo Pharmaceutical Co., Ltd.
01 1Hydrocortisone succinate
01 1Japan
Registration Number : 219MF10308
Registrant's Address : 2-6-2 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2007-10-05
Latest Date of Registration : 2007-10-05
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PharmaCompass offers a list of Hydrocortisone Sodium Succinate 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 Hydrocortisone Sodium Succinate manufacturer or Hydrocortisone Sodium Succinate supplier for your needs.
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PharmaCompass also assists you with knowing the Hydrocortisone Sodium Succinate API Price utilized in the formulation of products. Hydrocortisone Sodium Succinate API Price is not always fixed or binding as the Hydrocortisone Sodium Succinate Price is obtained through a variety of data sources. The Hydrocortisone Sodium Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Solu-Cortef manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solu-Cortef, including repackagers and relabelers. The FDA regulates Solu-Cortef manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solu-Cortef 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 Solu-Cortef manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Solu-Cortef supplier is an individual or a company that provides Solu-Cortef active pharmaceutical ingredient (API) or Solu-Cortef finished formulations upon request. The Solu-Cortef suppliers may include Solu-Cortef API manufacturers, exporters, distributors and traders.
click here to find a list of Solu-Cortef 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 Solu-Cortef Drug Master File in Japan (Solu-Cortef JDMF) empowers Solu-Cortef 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 Solu-Cortef JDMF during the approval evaluation for pharmaceutical products. At the time of Solu-Cortef JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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