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
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PharmaCompass offers a list of Cefminox Sodium 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 Cefminox Sodium manufacturer or Cefminox Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Cefminox Sodium API Price utilized in the formulation of products. Cefminox Sodium API Price is not always fixed or binding as the Cefminox Sodium Price is obtained through a variety of data sources. The Cefminox Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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.
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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.
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