01 1Inner Mongolia Changsheng Pharmaceutical Co. , Ltd.
01 1Benzylpenicillin Potassium
01 1China
Registration Number : 226MF10047
Registrant's Address : Industry Zone, Tuoketuo, Hohhot, Inner Mongolia, China
Initial Date of Registration : 2014-02-20
Latest Date of Registration : 2018-01-18
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PharmaCompass offers a list of Benzyl Penicillin 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 Benzyl Penicillin manufacturer or Benzyl Penicillin supplier for your needs.
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PharmaCompass also assists you with knowing the Benzyl Penicillin API Price utilized in the formulation of products. Benzyl Penicillin API Price is not always fixed or binding as the Benzyl Penicillin Price is obtained through a variety of data sources. The Benzyl Penicillin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cillora manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cillora, including repackagers and relabelers. The FDA regulates Cillora manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cillora 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 Cillora supplier is an individual or a company that provides Cillora active pharmaceutical ingredient (API) or Cillora finished formulations upon request. The Cillora suppliers may include Cillora API manufacturers, exporters, distributors and traders.
click here to find a list of Cillora 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 Cillora Drug Master File in Japan (Cillora JDMF) empowers Cillora 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 Cillora JDMF during the approval evaluation for pharmaceutical products. At the time of Cillora 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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