01 1Siegfried Evionnaz SA
01 1Hydrochloric acid prilocaine
01 1Switzerland
Registration Number : 219MF10013
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2007-01-18
Latest Date of Registration : 2022-05-25
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PharmaCompass offers a list of Prilocaine Hydrochloride 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 Prilocaine Hydrochloride manufacturer or Prilocaine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prilocaine Hydrochloride manufacturer or Prilocaine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Prilocaine Hydrochloride API Price utilized in the formulation of products. Prilocaine Hydrochloride API Price is not always fixed or binding as the Prilocaine Hydrochloride Price is obtained through a variety of data sources. The Prilocaine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Xylonest manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xylonest, including repackagers and relabelers. The FDA regulates Xylonest manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xylonest API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Xylonest supplier is an individual or a company that provides Xylonest active pharmaceutical ingredient (API) or Xylonest finished formulations upon request. The Xylonest suppliers may include Xylonest API manufacturers, exporters, distributors and traders.
click here to find a list of Xylonest 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 Xylonest Drug Master File in Japan (Xylonest JDMF) empowers Xylonest 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 Xylonest JDMF during the approval evaluation for pharmaceutical products. At the time of Xylonest JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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