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PharmaCompass offers a list of Ceftriaxone 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 Ceftriaxone manufacturer or Ceftriaxone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ceftriaxone manufacturer or Ceftriaxone supplier.
PharmaCompass also assists you with knowing the Ceftriaxone API Price utilized in the formulation of products. Ceftriaxone API Price is not always fixed or binding as the Ceftriaxone Price is obtained through a variety of data sources. The Ceftriaxone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Biotrakson manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Biotrakson, including repackagers and relabelers. The FDA regulates Biotrakson manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Biotrakson 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 Biotrakson manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Biotrakson supplier is an individual or a company that provides Biotrakson active pharmaceutical ingredient (API) or Biotrakson finished formulations upon request. The Biotrakson suppliers may include Biotrakson API manufacturers, exporters, distributors and traders.
click here to find a list of Biotrakson 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 Biotrakson Drug Master File in Japan (Biotrakson JDMF) empowers Biotrakson 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 Biotrakson JDMF during the approval evaluation for pharmaceutical products. At the time of Biotrakson 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 Biotrakson suppliers with JDMF on PharmaCompass.
We have 9 companies offering Biotrakson
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