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