01 1Sekisui Medical Co., Ltd.
01 1Indigo carmine
01 1Japan
Registration Number : 217MF10769
Registrant's Address : 2-1-3 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-20
Latest Date of Registration : 2009-07-09
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PharmaCompass offers a list of Indigo Carmine 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 Indigo Carmine manufacturer or Indigo Carmine supplier for your needs.
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PharmaCompass also assists you with knowing the Indigo Carmine API Price utilized in the formulation of products. Indigo Carmine API Price is not always fixed or binding as the Indigo Carmine Price is obtained through a variety of data sources. The Indigo Carmine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Indigotindisulfonate Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Indigotindisulfonate Sodium, including repackagers and relabelers. The FDA regulates Indigotindisulfonate Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Indigotindisulfonate Sodium API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Indigotindisulfonate Sodium supplier is an individual or a company that provides Indigotindisulfonate Sodium active pharmaceutical ingredient (API) or Indigotindisulfonate Sodium finished formulations upon request. The Indigotindisulfonate Sodium suppliers may include Indigotindisulfonate Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Indigotindisulfonate Sodium 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 Indigotindisulfonate Sodium Drug Master File in Japan (Indigotindisulfonate Sodium JDMF) empowers Indigotindisulfonate Sodium 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 Indigotindisulfonate Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Indigotindisulfonate Sodium JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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