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 Benzylpenicillin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzylpenicillin Sodium, including repackagers and relabelers. The FDA regulates Benzylpenicillin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzylpenicillin 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 Benzylpenicillin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benzylpenicillin Sodium supplier is an individual or a company that provides Benzylpenicillin Sodium active pharmaceutical ingredient (API) or Benzylpenicillin Sodium finished formulations upon request. The Benzylpenicillin Sodium suppliers may include Benzylpenicillin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Benzylpenicillin 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 Benzylpenicillin Sodium Drug Master File in Japan (Benzylpenicillin Sodium JDMF) empowers Benzylpenicillin 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 Benzylpenicillin Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Benzylpenicillin 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 Benzylpenicillin Sodium suppliers with JDMF on PharmaCompass.
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