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 Torii-no, 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, 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.
A Tensobon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tensobon, including repackagers and relabelers. The FDA regulates Tensobon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tensobon 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 Tensobon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Tensobon supplier is an individual or a company that provides Tensobon active pharmaceutical ingredient (API) or Tensobon finished formulations upon request. The Tensobon suppliers may include Tensobon API manufacturers, exporters, distributors and traders.
click here to find a list of Tensobon 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 Tensobon Drug Master File in Japan (Tensobon JDMF) empowers Tensobon 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 Tensobon JDMF during the approval evaluation for pharmaceutical products. At the time of Tensobon 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 Tensobon suppliers with JDMF on PharmaCompass.
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