01 1Daito Co., Ltd.
02 1EISAI PHARMACEUTICALS INDIA PVT LTD
03 2Jiangxi Synergy Pharmaceutical Co. , Ltd.
04 1Kongo Chemical Co., Ltd.
05 1Kyongbo Pharmaceutical Co. , Ltd.
06 1Matrix Pharmacorp Private Limited
07 2Zhejiang Tianyu Pharmaceutical Co. , Ltd.
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PharmaCompass offers a list of Azilsartan 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 Azilsartan manufacturer or Azilsartan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azilsartan manufacturer or Azilsartan supplier.
PharmaCompass also assists you with knowing the Azilsartan API Price utilized in the formulation of products. Azilsartan API Price is not always fixed or binding as the Azilsartan Price is obtained through a variety of data sources. The Azilsartan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Edarbi manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Edarbi, including repackagers and relabelers. The FDA regulates Edarbi manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Edarbi 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 Edarbi manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Edarbi supplier is an individual or a company that provides Edarbi active pharmaceutical ingredient (API) or Edarbi finished formulations upon request. The Edarbi suppliers may include Edarbi API manufacturers, exporters, distributors and traders.
click here to find a list of Edarbi 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 Edarbi Drug Master File in Japan (Edarbi JDMF) empowers Edarbi 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 Edarbi JDMF during the approval evaluation for pharmaceutical products. At the time of Edarbi 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 Edarbi suppliers with JDMF on PharmaCompass.
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