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.
01 1Dedicated to tolvaptan production
02 4Tolvaptan
03 1Tolvaptan "D"
04 1Tolvaptan (amorphous) (manufacturing only)
05 1Tolvaptan (manufacturing only)
01 1India
02 4Japan
03 2South Korea
04 1Taiwan
Registration Number : 303MF10018
Registrant's Address : Osaka Prefecture, Osaka City, Suminoe Ward, Nanko Kita 1-19-40
Initial Date of Registration : 2021-01-26
Latest Date of Registration : 2021-01-26
Registration Number : 301MF10051
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2019-08-20
Latest Date of Registration : 2019-08-20
Registration Number : 303MF10006
Registrant's Address : 343, Sapyeong-daero, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2021-01-14
Latest Date of Registration : 2021-01-14
Registration Number : 303MF10013
Registrant's Address : 161, Yeoksam-ro, Gangnam-gu, Seoul, Korea
Initial Date of Registration : 2021-01-26
Latest Date of Registration : 2021-01-26
Registration Number : 302MF10134
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2020-11-04
Latest Date of Registration : 2020-11-04
Tolvaptan (amorphous) (for manufacturing purposes only)
Registration Number : 303MF10049
Registrant's Address : 129 Suidocho, Aoi Ward, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2021-03-22
Latest Date of Registration : 2021-03-22
Tolvaptan (for manufacturing only)
Registration Number : 302MF10158
Registrant's Address : 129 Suidocho, Aoi Ward, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2020-12-23
Latest Date of Registration : 2021-02-05
Registration Number : 302MF10031
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2020-02-20
Latest Date of Registration : 2020-02-20
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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.
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