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