01 1HETERO DRUGS LIMITED.
02 1Hamari PFST Co., Ltd.
03 1JEIL PHARMACEUTICAL CO. , LTD.
04 1Shin Poong Pharm. Co. , Ltd.
05 1Shiratori Pharmaceutical Co., Ltd.
06 2Shizuoka Caffeine Industry Co., Ltd.
07 1Syn-Tech Chem. & Pharm. Co. , Ltd.
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PharmaCompass offers a list of Tolvaptan 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 Tolvaptan manufacturer or Tolvaptan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tolvaptan manufacturer or Tolvaptan supplier.
PharmaCompass also assists you with knowing the Tolvaptan API Price utilized in the formulation of products. Tolvaptan API Price is not always fixed or binding as the Tolvaptan Price is obtained through a variety of data sources. The Tolvaptan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Samsca manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Samsca, including repackagers and relabelers. The FDA regulates Samsca manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Samsca 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 Samsca manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Samsca supplier is an individual or a company that provides Samsca active pharmaceutical ingredient (API) or Samsca finished formulations upon request. The Samsca suppliers may include Samsca API manufacturers, exporters, distributors and traders.
click here to find a list of Samsca 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 Samsca Drug Master File in Japan (Samsca JDMF) empowers Samsca 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 Samsca JDMF during the approval evaluation for pharmaceutical products. At the time of Samsca 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 Samsca suppliers with JDMF on PharmaCompass.
We have 7 companies offering Samsca
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