01 1Antibio(')ticos do Brazil Ltda
01 1Cephalothin sodium
01 1Brazil
Registration Number : 219MF10341
Registrant's Address : Rodovia Professor Zeferino Vaz,SP-332 Km 135 Cosmo(')polis-SP-Brazil ZpC 13151-350
Initial Date of Registration : 2007-11-21
Latest Date of Registration : 2020-06-11
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PharmaCompass offers a list of Cefalotin sodium Sterile 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 Cefalotin sodium Sterile manufacturer or Cefalotin sodium Sterile supplier for your needs.
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PharmaCompass also assists you with knowing the Cefalotin sodium Sterile API Price utilized in the formulation of products. Cefalotin sodium Sterile API Price is not always fixed or binding as the Cefalotin sodium Sterile Price is obtained through a variety of data sources. The Cefalotin sodium Sterile Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Seffin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Seffin, including repackagers and relabelers. The FDA regulates Seffin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Seffin 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 Seffin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Seffin supplier is an individual or a company that provides Seffin active pharmaceutical ingredient (API) or Seffin finished formulations upon request. The Seffin suppliers may include Seffin API manufacturers, exporters, distributors and traders.
click here to find a list of Seffin 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 Seffin Drug Master File in Japan (Seffin JDMF) empowers Seffin 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 Seffin JDMF during the approval evaluation for pharmaceutical products. At the time of Seffin 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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