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
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.
click here to find a list of Penicillin G Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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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