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 purposes only)
Registration Number : 217MF11222
Registrant's Address : 121-15 Torino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2015-11-02
Japanese Pharmacopoeia Captopril (for manufacturing purposes 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
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PharmaCompass offers a list of Captopril 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 Captopril manufacturer or Captopril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Captopril manufacturer or Captopril supplier.
PharmaCompass also assists you with knowing the Captopril API Price utilized in the formulation of products. Captopril API Price is not always fixed or binding as the Captopril Price is obtained through a variety of data sources. The Captopril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tensiomin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tensiomin, including repackagers and relabelers. The FDA regulates Tensiomin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tensiomin 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 Tensiomin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tensiomin supplier is an individual or a company that provides Tensiomin active pharmaceutical ingredient (API) or Tensiomin finished formulations upon request. The Tensiomin suppliers may include Tensiomin API manufacturers, exporters, distributors and traders.
click here to find a list of Tensiomin 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 Tensiomin Drug Master File in Japan (Tensiomin JDMF) empowers Tensiomin 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 Tensiomin JDMF during the approval evaluation for pharmaceutical products. At the time of Tensiomin 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 Tensiomin suppliers with JDMF on PharmaCompass.
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