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.
01 1Azil sartan
02 7Azilsartan
03 1Azilsartan (manufacturing only)
01 4China
02 3Japan
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, Anaka...
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, County, 330700, Yichun City, Jiangxi Provin...
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, County, 330700, Yichun City, Jiangxi Provin...
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 : 2025-06-04
Azilsartan (for manufacturing purposes only)
Registration Number : 304MF10020
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2022-01-26
Latest Date of Registration : 2022-11-16
Registration Number : 301MF10062
Registrant's Address : Plot No. 14, 99 and 100, IDA, Pashamylaram Phase-II, Patancheru, Sangareddy District ...
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
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PharmaCompass offers a list of Azilsartan Medoxomil Potassium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Azilsartan Medoxomil Potassium manufacturer or Azilsartan Medoxomil Potassium supplier for your needs.
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A Azilsartan Medoxomil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azilsartan Medoxomil, including repackagers and relabelers. The FDA regulates Azilsartan Medoxomil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azilsartan Medoxomil 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 Medoxomil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Azilsartan Medoxomil supplier is an individual or a company that provides Azilsartan Medoxomil active pharmaceutical ingredient (API) or Azilsartan Medoxomil finished formulations upon request. The Azilsartan Medoxomil suppliers may include Azilsartan Medoxomil API manufacturers, exporters, distributors and traders.
click here to find a list of Azilsartan Medoxomil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Medoxomil Drug Master File in Japan (Azilsartan Medoxomil JDMF) empowers Azilsartan Medoxomil 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 Medoxomil JDMF during the approval evaluation for pharmaceutical products. At the time of Azilsartan Medoxomil 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 Medoxomil suppliers with JDMF on PharmaCompass.
We have 7 companies offering Azilsartan Medoxomil
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