01 1Siegfried (Nantong) Pharmaceuticals Co. , Ltd.
02 1Siegfried Ltd
01 2Primidone
01 2Switzerland
Registration Number : 226MF10113
Registrant's Address : Untere Bru(¨)hlstrasse 4,CH-4800 Zofingen Switzerland
Initial Date of Registration : 2014-05-29
Latest Date of Registration : 2014-05-29
Registration Number : 306MF10004
Registrant's Address : No. 5, Tongshun Road, Nantong Economic & Technological Development Area, Nantong, Jia...
Initial Date of Registration : 2024-01-11
Latest Date of Registration : 2024-01-11
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PharmaCompass offers a list of Primidone 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 Primidone manufacturer or Primidone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Primidone manufacturer or Primidone supplier.
PharmaCompass also assists you with knowing the Primidone API Price utilized in the formulation of products. Primidone API Price is not always fixed or binding as the Primidone Price is obtained through a variety of data sources. The Primidone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mylepsinum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mylepsinum, including repackagers and relabelers. The FDA regulates Mylepsinum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mylepsinum 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 Mylepsinum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mylepsinum supplier is an individual or a company that provides Mylepsinum active pharmaceutical ingredient (API) or Mylepsinum finished formulations upon request. The Mylepsinum suppliers may include Mylepsinum API manufacturers, exporters, distributors and traders.
click here to find a list of Mylepsinum 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 Mylepsinum Drug Master File in Japan (Mylepsinum JDMF) empowers Mylepsinum 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 Mylepsinum JDMF during the approval evaluation for pharmaceutical products. At the time of Mylepsinum 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 Mylepsinum suppliers with JDMF on PharmaCompass.
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