01 1Shandong Anhong Pharmaceutical Co. , Ltd.
01 1Sef Mino box sodium (sterile)
01 1China
Registration Number : 227MF10283
Registrant's Address : No. 29 Huayuan Street Linyi County, Dezhou, Shandong, China
Initial Date of Registration : 2015-12-15
Latest Date of Registration : 2015-12-15
A Cefminox Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefminox Sodium, including repackagers and relabelers. The FDA regulates Cefminox Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefminox Sodium 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 Cefminox Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cefminox Sodium supplier is an individual or a company that provides Cefminox Sodium active pharmaceutical ingredient (API) or Cefminox Sodium finished formulations upon request. The Cefminox Sodium suppliers may include Cefminox Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Cefminox Sodium 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 Cefminox Sodium Drug Master File in Japan (Cefminox Sodium JDMF) empowers Cefminox Sodium 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 Cefminox Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Cefminox Sodium 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 Cefminox Sodium suppliers with JDMF on PharmaCompass.
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