01 1Sumitomo Chemical Co., Ltd.
01 1Japanese Pharmacopoeia propylthiouracil
01 1Japan
Japanese Pharmacopoeia Propylthiouracil
Registration Number : 217MF10086
Registrant's Address : 2-27-1 Shinkawa, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-23
Latest Date of Registration : 2007-09-06
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PharmaCompass offers a list of Propylthiouracil 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 Propylthiouracil manufacturer or Propylthiouracil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propylthiouracil manufacturer or Propylthiouracil supplier.
PharmaCompass also assists you with knowing the Propylthiouracil API Price utilized in the formulation of products. Propylthiouracil API Price is not always fixed or binding as the Propylthiouracil Price is obtained through a variety of data sources. The Propylthiouracil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PTU manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PTU, including repackagers and relabelers. The FDA regulates PTU manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PTU 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 PTU manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PTU supplier is an individual or a company that provides PTU active pharmaceutical ingredient (API) or PTU finished formulations upon request. The PTU suppliers may include PTU API manufacturers, exporters, distributors and traders.
click here to find a list of PTU 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 PTU Drug Master File in Japan (PTU JDMF) empowers PTU 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 PTU JDMF during the approval evaluation for pharmaceutical products. At the time of PTU 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 PTU suppliers with JDMF on PharmaCompass.
