01 3China Chemical Co., Ltd.
02 1Dottikon Exclusive Synthesis AG
03 1Muromachi Chemical Co., Ltd.
01 1Isosorbide dinitrate 20% solution
02 1Isosorbide dinitrate 20% solution Chuka
03 1Isosorbide dinitrate 25% Chichuka
04 1Isosorbide dinitrate 40% Chichuka
05 1Nitrate isosorbitol 40% powder P1007.021
01 4Japan
02 1Switzerland
Isosorbide dinitrate 25% dispersion
Registration Number : 217MF10796
Registrant's Address : 1-6 Tenno Shioyacho, Kure City, Hiroshima Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2007-04-27
Isosorbide dinitrate 20% solution
Registration Number : 217MF10797
Registrant's Address : 1-6 Tenno Shioyacho, Kure City, Hiroshima Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2009-06-16
Isosorbide dinitrate 40% dispersion
Registration Number : 217MF10795
Registrant's Address : 1-6 Tenno Shioyacho, Kure City, Hiroshima Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2006-05-18
Isosorbitol nitrate 40% powder P1007.021
Registration Number : 217MF11278
Registrant's Address : Hembrunnstr. 17, CH-5605 Dottikon, Switzerland
Initial Date of Registration : 2005-12-20
Latest Date of Registration : 2008-03-28
Isosorbide dinitrate 20% solution
Registration Number : 217MF10572
Registrant's Address : 1-38-5 Shinshotatecho, Omuta City, Fukuoka Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2009-06-02
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PharmaCompass offers a list of Isosorbide Dinitrate 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 Isosorbide Dinitrate manufacturer or Isosorbide Dinitrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isosorbide Dinitrate manufacturer or Isosorbide Dinitrate supplier.
PharmaCompass also assists you with knowing the Isosorbide Dinitrate API Price utilized in the formulation of products. Isosorbide Dinitrate API Price is not always fixed or binding as the Isosorbide Dinitrate Price is obtained through a variety of data sources. The Isosorbide Dinitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sorbitrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sorbitrate, including repackagers and relabelers. The FDA regulates Sorbitrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sorbitrate 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 Sorbitrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sorbitrate supplier is an individual or a company that provides Sorbitrate active pharmaceutical ingredient (API) or Sorbitrate finished formulations upon request. The Sorbitrate suppliers may include Sorbitrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sorbitrate 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 Sorbitrate Drug Master File in Japan (Sorbitrate JDMF) empowers Sorbitrate 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 Sorbitrate JDMF during the approval evaluation for pharmaceutical products. At the time of Sorbitrate 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 Sorbitrate suppliers with JDMF on PharmaCompass.
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