01 1Hebei Shengxue Dacheng Pharmaceutical Co. , Ltd.
01 1Streptomycin sulfate
01 1China
Registration Number : 229MF10076
Registrant's Address : No. 50 Shengxue Road, Luncheng Shijiazhuang, Hebei Province, China
Initial Date of Registration : 2017-04-11
Latest Date of Registration : 2017-04-11
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PharmaCompass offers a list of Streptomycin 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 Streptomycin manufacturer or Streptomycin supplier for your needs.
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PharmaCompass also assists you with knowing the Streptomycin API Price utilized in the formulation of products. Streptomycin API Price is not always fixed or binding as the Streptomycin Price is obtained through a variety of data sources. The Streptomycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Estreptomicina CEPA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estreptomicina CEPA, including repackagers and relabelers. The FDA regulates Estreptomicina CEPA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estreptomicina CEPA 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 Estreptomicina CEPA supplier is an individual or a company that provides Estreptomicina CEPA active pharmaceutical ingredient (API) or Estreptomicina CEPA finished formulations upon request. The Estreptomicina CEPA suppliers may include Estreptomicina CEPA API manufacturers, exporters, distributors and traders.
click here to find a list of Estreptomicina CEPA 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 Estreptomicina CEPA Drug Master File in Japan (Estreptomicina CEPA JDMF) empowers Estreptomicina CEPA 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 Estreptomicina CEPA JDMF during the approval evaluation for pharmaceutical products. At the time of Estreptomicina CEPA 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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