01 1Kaken Pharmaceutical Co., Ltd.
01 1Pronase
01 1Japan
Registration Number : 217MF10390
Registrant's Address : 2-28-8 Honkomagome, Bunkyo-ku, Tokyo
Initial Date of Registration : 2005-07-27
Latest Date of Registration : 2009-11-09
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PharmaCompass offers a list of Tolazamide 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 Tolazamide manufacturer or Tolazamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tolazamide manufacturer or Tolazamide supplier.
PharmaCompass also assists you with knowing the Tolazamide API Price utilized in the formulation of products. Tolazamide API Price is not always fixed or binding as the Tolazamide Price is obtained through a variety of data sources. The Tolazamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tolazamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tolazamide, including repackagers and relabelers. The FDA regulates Tolazamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tolazamide 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 Tolazamide supplier is an individual or a company that provides Tolazamide active pharmaceutical ingredient (API) or Tolazamide finished formulations upon request. The Tolazamide suppliers may include Tolazamide API manufacturers, exporters, distributors and traders.
click here to find a list of Tolazamide 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 Tolazamide Drug Master File in Japan (Tolazamide JDMF) empowers Tolazamide 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 Tolazamide JDMF during the approval evaluation for pharmaceutical products. At the time of Tolazamide 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 Tolazamide suppliers with JDMF on PharmaCompass.
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