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01 RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A. (1)
01 Dimenhydrinate (1)
01 Italy (1)
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PharmaCompass offers a list of Dimenhydrinate 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 Dimenhydrinate manufacturer or Dimenhydrinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimenhydrinate manufacturer or Dimenhydrinate supplier.
PharmaCompass also assists you with knowing the Dimenhydrinate API Price utilized in the formulation of products. Dimenhydrinate API Price is not always fixed or binding as the Dimenhydrinate Price is obtained through a variety of data sources. The Dimenhydrinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dimenidrinato manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dimenidrinato, including repackagers and relabelers. The FDA regulates Dimenidrinato manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dimenidrinato 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 Dimenidrinato manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dimenidrinato supplier is an individual or a company that provides Dimenidrinato active pharmaceutical ingredient (API) or Dimenidrinato finished formulations upon request. The Dimenidrinato suppliers may include Dimenidrinato API manufacturers, exporters, distributors and traders.
click here to find a list of Dimenidrinato 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 Dimenidrinato Drug Master File in Japan (Dimenidrinato JDMF) empowers Dimenidrinato 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 Dimenidrinato JDMF during the approval evaluation for pharmaceutical products. At the time of Dimenidrinato 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 Dimenidrinato suppliers with JDMF on PharmaCompass.
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