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PharmaCompass offers a list of Famciclovir 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 Famciclovir manufacturer or Famciclovir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Famciclovir manufacturer or Famciclovir supplier.
PharmaCompass also assists you with knowing the Famciclovir API Price utilized in the formulation of products. Famciclovir API Price is not always fixed or binding as the Famciclovir Price is obtained through a variety of data sources. The Famciclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Famciclovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Famciclovir, including repackagers and relabelers. The FDA regulates Famciclovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Famciclovir 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 Famciclovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Famciclovir supplier is an individual or a company that provides Famciclovir active pharmaceutical ingredient (API) or Famciclovir finished formulations upon request. The Famciclovir suppliers may include Famciclovir API manufacturers, exporters, distributors and traders.
click here to find a list of Famciclovir 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 Famciclovir Drug Master File in Japan (Famciclovir JDMF) empowers Famciclovir 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 Famciclovir JDMF during the approval evaluation for pharmaceutical products. At the time of Famciclovir 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 Famciclovir suppliers with JDMF on PharmaCompass.
We have 5 companies offering Famciclovir
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