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 Torii-no, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-12-01
26
PharmaCompass offers a list of Trandolapril 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 Trandolapril manufacturer or Trandolapril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trandolapril manufacturer or Trandolapril supplier.
A Trandolaprilum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trandolaprilum, including repackagers and relabelers. The FDA regulates Trandolaprilum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trandolaprilum 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 Trandolaprilum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Trandolaprilum supplier is an individual or a company that provides Trandolaprilum active pharmaceutical ingredient (API) or Trandolaprilum finished formulations upon request. The Trandolaprilum suppliers may include Trandolaprilum API manufacturers, exporters, distributors and traders.
click here to find a list of Trandolaprilum 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 Trandolaprilum Drug Master File in Japan (Trandolaprilum JDMF) empowers Trandolaprilum 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 Trandolaprilum JDMF during the approval evaluation for pharmaceutical products. At the time of Trandolaprilum 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 Trandolaprilum suppliers with JDMF on PharmaCompass.
We have 2 companies offering Trandolaprilum
Get in contact with the supplier of your choice:
