01 1HAS Healthcare Advanced Synthesis SA
02 1Kyongbo Pharmaceutical Co. , Ltd.
03 1Shiratori Pharmaceutical Co., Ltd.
01 1Dedicated to the production of palonosetron hydrochloride
02 1Palonosetron Hydrochloride
03 1Palonosetron hydrochloride
01 1Japan
02 1South Korea
03 1Switzerland
Registration Number : 220MF10072
Registrant's Address : Via Industria, 24 6710 Biasca Switzerland
Initial Date of Registration : 2008-03-14
Latest Date of Registration : 2009-06-16
Registration Number : 304MF10110
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2022-08-03
Latest Date of Registration : 2022-08-03
Palonosetron Hydrochloride For manufacturing purposes only
Registration Number : 302MF10012
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2020-01-24
Latest Date of Registration : 2020-01-24
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PharmaCompass offers a list of Palonosetron 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 Palonosetron manufacturer or Palonosetron supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Palonosetron manufacturer or Palonosetron supplier.
PharmaCompass also assists you with knowing the Palonosetron API Price utilized in the formulation of products. Palonosetron API Price is not always fixed or binding as the Palonosetron Price is obtained through a variety of data sources. The Palonosetron Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CS-0621 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CS-0621, including repackagers and relabelers. The FDA regulates CS-0621 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CS-0621 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 CS-0621 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CS-0621 supplier is an individual or a company that provides CS-0621 active pharmaceutical ingredient (API) or CS-0621 finished formulations upon request. The CS-0621 suppliers may include CS-0621 API manufacturers, exporters, distributors and traders.
click here to find a list of CS-0621 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 CS-0621 Drug Master File in Japan (CS-0621 JDMF) empowers CS-0621 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 CS-0621 JDMF during the approval evaluation for pharmaceutical products. At the time of CS-0621 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 CS-0621 suppliers with JDMF on PharmaCompass.
We have 3 companies offering CS-0621
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