01 1Aurisco Pharmaceutical Co. , Ltd.
02 1Hetero Labs Limited
01 2Eplerenone
01 1China
02 1India
Registration Number : 304MF10019
Registrant's Address : Badu Industrial Park Zone, Tiantai, Zhejiang province, 317200, P. R. China
Initial Date of Registration : 2022-01-26
Latest Date of Registration : 2022-01-26
Registration Number : 304MF10031
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2022-02-10
Latest Date of Registration : 2022-02-10
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PharmaCompass offers a list of Eplerenone 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 Eplerenone manufacturer or Eplerenone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Eplerenone manufacturer or Eplerenone supplier.
PharmaCompass also assists you with knowing the Eplerenone API Price utilized in the formulation of products. Eplerenone API Price is not always fixed or binding as the Eplerenone Price is obtained through a variety of data sources. The Eplerenone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Selara manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selara, including repackagers and relabelers. The FDA regulates Selara manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selara 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 Selara manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selara supplier is an individual or a company that provides Selara active pharmaceutical ingredient (API) or Selara finished formulations upon request. The Selara suppliers may include Selara API manufacturers, exporters, distributors and traders.
click here to find a list of Selara 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 Selara Drug Master File in Japan (Selara JDMF) empowers Selara 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 Selara JDMF during the approval evaluation for pharmaceutical products. At the time of Selara 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 Selara suppliers with JDMF on PharmaCompass.
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