01 1Daiwa Pharmaceutical Industries 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 1Tianish Laboratories Private Limited
07 1Tokuyama Corporation
08 2Zhejiang Tianyu Pharmaceutical Co. , Ltd.
01 1Azil sartan
02 8Azilsartan
03 1Azilsartan (manufacturing only)
01 4China
02 4Japan
03 1South Korea
04 1U.S.A
Registration Number : 305MF10020
Registrant's Address : Ⅴisakha PharmaCity Limited (SEZ), Plot Nos. 96,97,98,124&126, Parawada-531 019, Ana...
Initial Date of Registration : 2023-02-08
Latest Date of Registration : 2023-02-08
Registration Number : 305MF10141
Registrant's Address : Jiangxi Fengxin Industrial Park, Fengxin, 330700, Jiangxi Province, P. R. China
Initial Date of Registration : 2023-12-22
Latest Date of Registration : 2023-12-22
Registration Number : 302MF10016
Registrant's Address : Jiangxi Fengxin Industrial Park, Fengxin, 330700, Jiangxi Province, P. R. China
Initial Date of Registration : 2020-01-31
Latest Date of Registration : 2021-05-24
Registration Number : 302MF10007
Registrant's Address : 3 Himata, Toyama City, Toyama Prefecture
Initial Date of Registration : 2020-01-10
Latest Date of Registration : 2023-01-11
Registration Number : 301MF10112
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2019-12-25
Latest Date of Registration : 2022-01-20
Azilsartan (for manufacturing only)
Registration Number : 304MF10020
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2022-01-26
Latest Date of Registration : 2022-11-16
Registration Number : 302MF10010
Registrant's Address : 1-1 Mikage-cho, Shunan City, Yamaguchi Prefecture
Initial Date of Registration : 2020-01-17
Latest Date of Registration : 2021-05-10
Registration Number : 301MF10062
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2019-09-11
Latest Date of Registration : 2019-09-11
Registration Number : 305MF10041
Registrant's Address : Jiangkou Development Zone, Huangyan, Taizhou City, Zhejiang Province, People's Republ...
Initial Date of Registration : 2023-03-29
Latest Date of Registration : 2024-11-13
Registration Number : 304MF10129
Registrant's Address : Jiangkou Development Zone, Huangyan, Taizhou City, Zhejiang Province, People's Republ...
Initial Date of Registration : 2022-09-08
Latest Date of Registration : 2022-09-08
A Azilsartan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azilsartan, including repackagers and relabelers. The FDA regulates Azilsartan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azilsartan 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 Azilsartan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azilsartan supplier is an individual or a company that provides Azilsartan active pharmaceutical ingredient (API) or Azilsartan finished formulations upon request. The Azilsartan suppliers may include Azilsartan API manufacturers, exporters, distributors and traders.
click here to find a list of Azilsartan 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 Azilsartan Drug Master File in Japan (Azilsartan JDMF) empowers Azilsartan 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 Azilsartan JDMF during the approval evaluation for pharmaceutical products. At the time of Azilsartan 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 Azilsartan suppliers with JDMF on PharmaCompass.
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