EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI FRANCE
02 2Tianjin Jinjin Pharmaceutical Co. , Ltd.
03 1Zhejiang Langhua Pharmaceutical Co. , Ltd.
01 4Spironolactone
01 3China
02 1France
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 218MF10382
Registrant's Address : 32 rue Alexandre Dumas 75011 Paris France
Initial Date of Registration : 2006-03-20
Latest Date of Registration : 2026-01-08
Registration Number : 227MF10291
Registrant's Address : Industrial zone of Zhangjiawo Town, Xiqing District Economic & Developing Area, Tianj...
Initial Date of Registration : 2015-12-24
Latest Date of Registration : 2015-12-24
Registration Number : 220MF10037
Registrant's Address : Industrial zone of Zhangjiawo Town, Xiqing District Economic & Developing Area, Tianj...
Initial Date of Registration : 2008-02-05
Latest Date of Registration : 2008-02-05
Registration Number : 231MF10058
Registrant's Address : Zhejiang provincial chemical and medical materials base Linhai zone, Linhai, Zhejiang...
Initial Date of Registration : 2019-02-25
Latest Date of Registration : 2019-02-25
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PharmaCompass offers a list of Spironolactone 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 Spironolactone manufacturer or Spironolactone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Spironolactone manufacturer or Spironolactone supplier.
PharmaCompass also assists you with knowing the Spironolactone API Price utilized in the formulation of products. Spironolactone API Price is not always fixed or binding as the Spironolactone Price is obtained through a variety of data sources. The Spironolactone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CID5833 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CID5833, including repackagers and relabelers. The FDA regulates CID5833 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CID5833 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 CID5833 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CID5833 supplier is an individual or a company that provides CID5833 active pharmaceutical ingredient (API) or CID5833 finished formulations upon request. The CID5833 suppliers may include CID5833 API manufacturers, exporters, distributors and traders.
click here to find a list of CID5833 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 CID5833 Drug Master File in Japan (CID5833 JDMF) empowers CID5833 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 CID5833 JDMF during the approval evaluation for pharmaceutical products. At the time of CID5833 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 CID5833 suppliers with JDMF on PharmaCompass.
We have 3 companies offering CID5833
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