01 1Fersinsa Gb S. A. de C. V.
01 1Benzylpenicillin Potassium
01 1Netherlands
Registration Number : 229MF10121
Registrant's Address : Carretera Saltillo-Mty km 12.5, Ramos Arizpe, Coahuela 25900, Mexico
Initial Date of Registration : 2017-07-11
Latest Date of Registration : 2018-04-23
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PharmaCompass offers a list of Benzylpenicillin 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 Benzylpenicillin Sodium manufacturer or Benzylpenicillin Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Benzylpenicillin Sodium API Price utilized in the formulation of products. Benzylpenicillin Sodium API Price is not always fixed or binding as the Benzylpenicillin Sodium Price is obtained through a variety of data sources. The Benzylpenicillin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Penicillin G Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Penicillin G Sodium, including repackagers and relabelers. The FDA regulates Penicillin G Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Penicillin G 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 Penicillin G Sodium supplier is an individual or a company that provides Penicillin G Sodium active pharmaceutical ingredient (API) or Penicillin G Sodium finished formulations upon request. The Penicillin G Sodium suppliers may include Penicillin G Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Penicillin G 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 Penicillin G Sodium Drug Master File in Japan (Penicillin G Sodium JDMF) empowers Penicillin G 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 Penicillin G Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Penicillin G 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 Penicillin G Sodium suppliers with JDMF on PharmaCompass.
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