01 1Shanghai Wonder Pharmaceutical Co. , Ltd.
02 1Shizuoka Caffeine Industry Co., Ltd.
01 1Diprophylline (production only)
02 1Japanese Pharmacopoeia Non-Pharmaceutical Standard Dyphylline (for manufacturing only)
01 1China
02 1Japan
Diprophylline (for manufacturing only)
Registration Number : 217MF10611
Registrant's Address : 129 Suidocho, Aoi Ward, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2023-12-22
Japanese Pharmacopoeia Non-Drug Standard Diprophylline (For manufacturing only)
Registration Number : 301MF10018
Registrant's Address : No. 298, Huachuang Road, Jinshan District, Shanghai, P. R. China
Initial Date of Registration : 2019-06-07
Latest Date of Registration : 2019-06-07
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PharmaCompass offers a list of Dyphylline 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 Dyphylline manufacturer or Dyphylline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dyphylline manufacturer or Dyphylline supplier.
PharmaCompass also assists you with knowing the Dyphylline API Price utilized in the formulation of products. Dyphylline API Price is not always fixed or binding as the Dyphylline Price is obtained through a variety of data sources. The Dyphylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dylix manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dylix, including repackagers and relabelers. The FDA regulates Dylix manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dylix 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 Dylix manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dylix supplier is an individual or a company that provides Dylix active pharmaceutical ingredient (API) or Dylix finished formulations upon request. The Dylix suppliers may include Dylix API manufacturers, exporters, distributors and traders.
click here to find a list of Dylix 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 Dylix Drug Master File in Japan (Dylix JDMF) empowers Dylix 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 Dylix JDMF during the approval evaluation for pharmaceutical products. At the time of Dylix 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 Dylix suppliers with JDMF on PharmaCompass.
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