01 1Manac Co., Ltd.
01 1Japanese Pharmacopoeia Furopuropion (production only)
01 1Japan
Japanese Pharmacopoeia Flopropion (for manufacturing purposes only)
Registration Number : 217MF10673
Registrant's Address : 92 Minooki-cho, Fukuyama City, Hiroshima Prefecture
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2007-12-19
88
PharmaCompass offers a list of Flopropione 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 Flopropione manufacturer or Flopropione supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flopropione manufacturer or Flopropione supplier.
PharmaCompass also assists you with knowing the Flopropione API Price utilized in the formulation of products. Flopropione API Price is not always fixed or binding as the Flopropione Price is obtained through a variety of data sources. The Flopropione Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 05V5NVB5Y1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 05V5NVB5Y1, including repackagers and relabelers. The FDA regulates 05V5NVB5Y1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 05V5NVB5Y1 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 05V5NVB5Y1 supplier is an individual or a company that provides 05V5NVB5Y1 active pharmaceutical ingredient (API) or 05V5NVB5Y1 finished formulations upon request. The 05V5NVB5Y1 suppliers may include 05V5NVB5Y1 API manufacturers, exporters, distributors and traders.
click here to find a list of 05V5NVB5Y1 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 05V5NVB5Y1 Drug Master File in Japan (05V5NVB5Y1 JDMF) empowers 05V5NVB5Y1 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 05V5NVB5Y1 JDMF during the approval evaluation for pharmaceutical products. At the time of 05V5NVB5Y1 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 05V5NVB5Y1 suppliers with JDMF on PharmaCompass.
We have 1 companies offering 05V5NVB5Y1
Get in contact with the supplier of your choice:
