01 1DYNAMIT NOBEL GmbH
02 2GELTECH Co. , Ltd.
03 1Kouki Co., Ltd.
04 2Kyokuyo Chemical Industry Co., Ltd.
05 1NOF Corporation
06 1Nippi Co., Ltd.
07 4Nitta Gelatin Co., Ltd.
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PharmaCompass offers a list of Nitroglycerin 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 Nitroglycerin manufacturer or Nitroglycerin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nitroglycerin manufacturer or Nitroglycerin supplier.
PharmaCompass also assists you with knowing the Nitroglycerin API Price utilized in the formulation of products. Nitroglycerin API Price is not always fixed or binding as the Nitroglycerin Price is obtained through a variety of data sources. The Nitroglycerin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sustak manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sustak, including repackagers and relabelers. The FDA regulates Sustak manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sustak 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 Sustak manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sustak supplier is an individual or a company that provides Sustak active pharmaceutical ingredient (API) or Sustak finished formulations upon request. The Sustak suppliers may include Sustak API manufacturers, exporters, distributors and traders.
click here to find a list of Sustak 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 Sustak Drug Master File in Japan (Sustak JDMF) empowers Sustak 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 Sustak JDMF during the approval evaluation for pharmaceutical products. At the time of Sustak 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 Sustak suppliers with JDMF on PharmaCompass.
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