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PharmaCompass offers a list of Diphenylpyraline 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 Diphenylpyraline manufacturer or Diphenylpyraline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diphenylpyraline manufacturer or Diphenylpyraline supplier.
PharmaCompass also assists you with knowing the Diphenylpyraline API Price utilized in the formulation of products. Diphenylpyraline API Price is not always fixed or binding as the Diphenylpyraline Price is obtained through a variety of data sources. The Diphenylpyraline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diphenylpyraline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diphenylpyraline, including repackagers and relabelers. The FDA regulates Diphenylpyraline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diphenylpyraline API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Diphenylpyraline supplier is an individual or a company that provides Diphenylpyraline active pharmaceutical ingredient (API) or Diphenylpyraline finished formulations upon request. The Diphenylpyraline suppliers may include Diphenylpyraline API manufacturers, exporters, distributors and traders.
click here to find a list of Diphenylpyraline 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 Diphenylpyraline Drug Master File in Japan (Diphenylpyraline JDMF) empowers Diphenylpyraline 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 Diphenylpyraline JDMF during the approval evaluation for pharmaceutical products. At the time of Diphenylpyraline 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 Diphenylpyraline suppliers with JDMF on PharmaCompass.
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