01 2Zhejiang Shenzhou Pharmaceutical Co. , Ltd.
01 1Canrenoate potassium
02 1Potassium Canrenoate
01 2China
Registration Number : 302MF10059
Registrant's Address : No. 14 Chuangcheng Nan Road 317300, Xianju, Zhejiang, China
Initial Date of Registration : 2020-05-25
Latest Date of Registration : 2020-05-25
Registration Number : 219MF10376
Registrant's Address : No. 14 Chuangcheng Nan Road 317300, Xianju, Zhejiang, China
Initial Date of Registration : 2007-12-19
Latest Date of Registration : 2007-12-19
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PharmaCompass offers a list of Canrenoate Potassium 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 Canrenoate Potassium manufacturer or Canrenoate Potassium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Canrenoate Potassium manufacturer or Canrenoate Potassium supplier.
PharmaCompass also assists you with knowing the Canrenoate Potassium API Price utilized in the formulation of products. Canrenoate Potassium API Price is not always fixed or binding as the Canrenoate Potassium Price is obtained through a variety of data sources. The Canrenoate Potassium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Venactone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Venactone, including repackagers and relabelers. The FDA regulates Venactone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Venactone 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 Venactone supplier is an individual or a company that provides Venactone active pharmaceutical ingredient (API) or Venactone finished formulations upon request. The Venactone suppliers may include Venactone API manufacturers, exporters, distributors and traders.
click here to find a list of Venactone 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 Venactone Drug Master File in Japan (Venactone JDMF) empowers Venactone 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 Venactone JDMF during the approval evaluation for pharmaceutical products. At the time of Venactone 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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