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01 1Inner Mongolia Changsheng Pharmaceutical Co. , Ltd.
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01 1Benzylpenicillin Potassium
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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 C16H18N2O4S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C16H18N2O4S, including repackagers and relabelers. The FDA regulates C16H18N2O4S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C16H18N2O4S 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 C16H18N2O4S manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C16H18N2O4S supplier is an individual or a company that provides C16H18N2O4S active pharmaceutical ingredient (API) or C16H18N2O4S finished formulations upon request. The C16H18N2O4S suppliers may include C16H18N2O4S API manufacturers, exporters, distributors and traders.
click here to find a list of C16H18N2O4S 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 C16H18N2O4S Drug Master File in Japan (C16H18N2O4S JDMF) empowers C16H18N2O4S 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 C16H18N2O4S JDMF during the approval evaluation for pharmaceutical products. At the time of C16H18N2O4S 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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