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