01 1Assia Chemical Industries Ltd.
02 1Hetero Labs Limited
03 2Jiangxi Synergy Pharmaceutical Co. , Ltd.
04 1KOLON LIFE SCIENCE, INC.
05 1Novartis Pharmaceutical Manufacturing LLC
06 1Ouchi Shinko Chemical Industry Co., Ltd.
07 1Procos S. p. A.
08 1Sanyo Chemical Research Institute Co., Ltd.
09 1Sun Chemical Co., Ltd.
10 1Takeda Pharmaceutical Company Limited
11 2Yungjin Pharm. Co. ,Ltd
12 1Zhejiang Huahai Pharmaceutical Co. , Ltd.
13 1Zhejiang Tianyu Pharmaceutical Co. , Ltd.
14 1Zhuhai Rundu Pharmaceutical Co. , Ltd.
A Candesartan Cilexetil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Candesartan Cilexetil, including repackagers and relabelers. The FDA regulates Candesartan Cilexetil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Candesartan Cilexetil 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 Candesartan Cilexetil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Candesartan Cilexetil supplier is an individual or a company that provides Candesartan Cilexetil active pharmaceutical ingredient (API) or Candesartan Cilexetil finished formulations upon request. The Candesartan Cilexetil suppliers may include Candesartan Cilexetil API manufacturers, exporters, distributors and traders.
click here to find a list of Candesartan Cilexetil 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 Candesartan Cilexetil Drug Master File in Japan (Candesartan Cilexetil JDMF) empowers Candesartan Cilexetil 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 Candesartan Cilexetil JDMF during the approval evaluation for pharmaceutical products. At the time of Candesartan Cilexetil 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 Candesartan Cilexetil suppliers with JDMF on PharmaCompass.
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