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
A Streptomycin Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Streptomycin Sulfate, including repackagers and relabelers. The FDA regulates Streptomycin Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Streptomycin Sulfate 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 Streptomycin Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Streptomycin Sulfate supplier is an individual or a company that provides Streptomycin Sulfate active pharmaceutical ingredient (API) or Streptomycin Sulfate finished formulations upon request. The Streptomycin Sulfate suppliers may include Streptomycin Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Streptomycin Sulfate 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 Streptomycin Sulfate Drug Master File in Japan (Streptomycin Sulfate JDMF) empowers Streptomycin Sulfate 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 Streptomycin Sulfate JDMF during the approval evaluation for pharmaceutical products. At the time of Streptomycin Sulfate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Streptomycin Sulfate suppliers with JDMF on PharmaCompass.
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