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01 1Sogo Pharmaceutical Co., Ltd.
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01 1Hydrocortisone succinate
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Sodium Succinate manufacturer or Hydrocortisone Sodium Succinate supplier.
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 Nositrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nositrol, including repackagers and relabelers. The FDA regulates Nositrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nositrol 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 Nositrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nositrol supplier is an individual or a company that provides Nositrol active pharmaceutical ingredient (API) or Nositrol finished formulations upon request. The Nositrol suppliers may include Nositrol API manufacturers, exporters, distributors and traders.
click here to find a list of Nositrol 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 Nositrol Drug Master File in Japan (Nositrol JDMF) empowers Nositrol 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 Nositrol JDMF during the approval evaluation for pharmaceutical products. At the time of Nositrol 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 Nositrol suppliers with JDMF on PharmaCompass.
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