01 1Sumitomo Chemical Co., Ltd.
01 1Japanese Pharmacopoeia propylthiouracil
01 1Japan
Japanese Pharmacopoeia Propylthiouracil
Registration Number : 217MF10086
Registrant's Address : 2-7-1 Nihonbashi, 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 BB 0242498 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BB 0242498, including repackagers and relabelers. The FDA regulates BB 0242498 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BB 0242498 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A BB 0242498 supplier is an individual or a company that provides BB 0242498 active pharmaceutical ingredient (API) or BB 0242498 finished formulations upon request. The BB 0242498 suppliers may include BB 0242498 API manufacturers, exporters, distributors and traders.
click here to find a list of BB 0242498 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 BB 0242498 Drug Master File in Japan (BB 0242498 JDMF) empowers BB 0242498 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 BB 0242498 JDMF during the approval evaluation for pharmaceutical products. At the time of BB 0242498 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 BB 0242498 suppliers with JDMF on PharmaCompass.
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