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PharmaCompass offers a list of Cetraxate 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 Cetraxate manufacturer or Cetraxate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cetraxate manufacturer or Cetraxate supplier.
PharmaCompass also assists you with knowing the Cetraxate API Price utilized in the formulation of products. Cetraxate API Price is not always fixed or binding as the Cetraxate Price is obtained through a variety of data sources. The Cetraxate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 08IT6P8VHY manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 08IT6P8VHY, including repackagers and relabelers. The FDA regulates 08IT6P8VHY manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 08IT6P8VHY 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 08IT6P8VHY supplier is an individual or a company that provides 08IT6P8VHY active pharmaceutical ingredient (API) or 08IT6P8VHY finished formulations upon request. The 08IT6P8VHY suppliers may include 08IT6P8VHY API manufacturers, exporters, distributors and traders.
click here to find a list of 08IT6P8VHY 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 08IT6P8VHY Drug Master File in Japan (08IT6P8VHY JDMF) empowers 08IT6P8VHY 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 08IT6P8VHY JDMF during the approval evaluation for pharmaceutical products. At the time of 08IT6P8VHY 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 08IT6P8VHY suppliers with JDMF on PharmaCompass.
We have 2 companies offering 08IT6P8VHY
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