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01 Siegfried Evionnaz SA (1)
01 Hydrochloric acid prilocaine (1)
01 Switzerland (1)
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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 Citanest manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Citanest, including repackagers and relabelers. The FDA regulates Citanest manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Citanest 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 Citanest manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Citanest supplier is an individual or a company that provides Citanest active pharmaceutical ingredient (API) or Citanest finished formulations upon request. The Citanest suppliers may include Citanest API manufacturers, exporters, distributors and traders.
click here to find a list of Citanest 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 Citanest Drug Master File in Japan (Citanest JDMF) empowers Citanest 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 Citanest JDMF during the approval evaluation for pharmaceutical products. At the time of Citanest 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 Citanest suppliers with JDMF on PharmaCompass.
