Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1CHUNGHWA CHEMICAL SYNTHESIS & BIOTECH CO. , LTD.
02 1Chunghwa Chemical Synthesis & Biotech Co. , Ltd.
03 1Ohara Pharmaceutical Co., Ltd.
01 3Trandolapril
01 1Japan
02 2Taiwan
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registration Number : 225MF10083
Registrant's Address : No. 1, Tung-Hsing St. , Shu-Lin, New Taipei City 23850, Taiwan
Initial Date of Registration : 2013-04-23
Latest Date of Registration : 2020-03-23
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Registration Number : 218MF10666
Registrant's Address : 1, Tung-Hsing, Street, Shu-Lin 238, Taipei Hsien, Taiwan, Republic of China
Initial Date of Registration : 2006-07-24
Latest Date of Registration : 2006-07-24
Registration Number : 217MF11216
Registrant's Address : 121-15 Toriiino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-12-01
A Trandolapril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trandolapril, including repackagers and relabelers. The FDA regulates Trandolapril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trandolapril 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 Trandolapril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trandolapril supplier is an individual or a company that provides Trandolapril active pharmaceutical ingredient (API) or Trandolapril finished formulations upon request. The Trandolapril suppliers may include Trandolapril API manufacturers, exporters, distributors and traders.
click here to find a list of Trandolapril 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 Trandolapril Drug Master File in Japan (Trandolapril JDMF) empowers Trandolapril 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 Trandolapril JDMF during the approval evaluation for pharmaceutical products. At the time of Trandolapril 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 Trandolapril suppliers with JDMF on PharmaCompass.
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