01 1Kyongbo Pharmaceutical Co. , Ltd.
02 1Ohara Pharmaceutical Co., Ltd.
03 1Osaka Synthetic Organic Chemical Research Institute, Inc.
01 1Hydrochloric acid imidapril
02 1Imidapril hydrochloride
03 1Only the Japanese Pharmacopoeia imidapril hydrochloride salt production
01 2Japan
02 1South Korea
Registration Number : 227MF10222
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2015-08-31
Latest Date of Registration : 2015-08-31
Registration Number : 219MF10095
Registrant's Address : 121-15 Torino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2007-03-14
Latest Date of Registration : 2007-03-14
Japanese Pharmacopoeia Imidapril Hydrochloride For manufacturing only
Registration Number : 221MF10285
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2009-12-22
Latest Date of Registration : 2020-12-07
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PharmaCompass offers a list of Imidapril 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 Imidapril manufacturer or Imidapril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Imidapril manufacturer or Imidapril supplier.
PharmaCompass also assists you with knowing the Imidapril API Price utilized in the formulation of products. Imidapril API Price is not always fixed or binding as the Imidapril Price is obtained through a variety of data sources. The Imidapril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tanatril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tanatril, including repackagers and relabelers. The FDA regulates Tanatril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tanatril 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 Tanatril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tanatril supplier is an individual or a company that provides Tanatril active pharmaceutical ingredient (API) or Tanatril finished formulations upon request. The Tanatril suppliers may include Tanatril API manufacturers, exporters, distributors and traders.
click here to find a list of Tanatril 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 Tanatril Drug Master File in Japan (Tanatril JDMF) empowers Tanatril 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 Tanatril JDMF during the approval evaluation for pharmaceutical products. At the time of Tanatril 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 Tanatril suppliers with JDMF on PharmaCompass.
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