01 1Jiangxi Dongfeng Pharmaceutical Co. , Ltd.
01 1BENZYLPENICILLIN BENZATHINE HYDRATE
01 1China
BENZYLPENICILLIN BENZATHINE HYDRATE
Registration Number : 219MF10336
Registrant's Address : 15 Dongfeng Rd. , Leping City, Jiangxi Province, China
Initial Date of Registration : 2007-11-21
Latest Date of Registration : 2007-11-21
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PharmaCompass offers a list of Penicillin G Benzathine 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 Penicillin G Benzathine manufacturer or Penicillin G Benzathine supplier for your needs.
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A Pendysin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pendysin, including repackagers and relabelers. The FDA regulates Pendysin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pendysin 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 Pendysin supplier is an individual or a company that provides Pendysin active pharmaceutical ingredient (API) or Pendysin finished formulations upon request. The Pendysin suppliers may include Pendysin API manufacturers, exporters, distributors and traders.
click here to find a list of Pendysin 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 Pendysin Drug Master File in Japan (Pendysin JDMF) empowers Pendysin 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 Pendysin JDMF during the approval evaluation for pharmaceutical products. At the time of Pendysin 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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