01 1Zhejiang Zhenyuan Pharmaceutical Co. , Ltd.
01 1Lornoxicam
01 1China
Registration Number : 221MF10209
Registrant's Address : No. 1015 Shengli West Road, Shaoxing City, Zhejiang, China
Initial Date of Registration : 2009-09-28
Latest Date of Registration : 2009-09-28
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PharmaCompass offers a list of Lornoxicam 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 Lornoxicam manufacturer or Lornoxicam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lornoxicam manufacturer or Lornoxicam supplier.
PharmaCompass also assists you with knowing the Lornoxicam API Price utilized in the formulation of products. Lornoxicam API Price is not always fixed or binding as the Lornoxicam Price is obtained through a variety of data sources. The Lornoxicam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Xefo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xefo, including repackagers and relabelers. The FDA regulates Xefo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xefo 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 Xefo manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Xefo supplier is an individual or a company that provides Xefo active pharmaceutical ingredient (API) or Xefo finished formulations upon request. The Xefo suppliers may include Xefo API manufacturers, exporters, distributors and traders.
click here to find a list of Xefo 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 Xefo Drug Master File in Japan (Xefo JDMF) empowers Xefo 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 Xefo JDMF during the approval evaluation for pharmaceutical products. At the time of Xefo 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 Xefo suppliers with JDMF on PharmaCompass.
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