01 1Ohara Pharmaceutical Co., Ltd.
02 1Shandong Weifang Pharmaceutical Factory Co. , Ltd.
03 1Zhejiang Huahai Pharmaceutical Co. , Ltd.
01 1Captopril
02 1Day stations captopril (production only)
03 1Japanese Pharmacopoeia captopril (production only)
01 2China
02 1Japan
Japanese Pharmacopoeia Captopril (for manufacturing only)
Registration Number : 217MF11222
Registrant's Address : 121-15 Toriiino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2015-11-02
JP Captopril (for manufacturing only)
Registration Number : 221MF10240
Registrant's Address : 1 Beijing Street west, Weifang, Shandong, China
Initial Date of Registration : 2009-11-09
Latest Date of Registration : 2009-11-09
Registration Number : 227MF10237
Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China
Initial Date of Registration : 2015-09-24
Latest Date of Registration : 2018-03-30
A Captopril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Captopril, including repackagers and relabelers. The FDA regulates Captopril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Captopril 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 Captopril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Captopril supplier is an individual or a company that provides Captopril active pharmaceutical ingredient (API) or Captopril finished formulations upon request. The Captopril suppliers may include Captopril API manufacturers, exporters, distributors and traders.
click here to find a list of Captopril 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 Captopril Drug Master File in Japan (Captopril JDMF) empowers Captopril 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 Captopril JDMF during the approval evaluation for pharmaceutical products. At the time of Captopril 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 Captopril suppliers with JDMF on PharmaCompass.
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