01 1Yanagishima Pharmaceutical Co., Ltd.
01 1Potassium iodide (production only)
01 1Blank
Potassium iodide (for manufacturing purposes only)
Registration Number : 218MF10333
Registrant's Address : 1-5-17 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2010-04-12
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PharmaCompass offers a list of Potassium Iodide 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 Potassium Iodide manufacturer or Potassium Iodide supplier for your needs.
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PharmaCompass also assists you with knowing the Potassium Iodide API Price utilized in the formulation of products. Potassium Iodide API Price is not always fixed or binding as the Potassium Iodide Price is obtained through a variety of data sources. The Potassium Iodide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Merck dura Brand of Potassium Iodide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Merck dura Brand of Potassium Iodide, including repackagers and relabelers. The FDA regulates Merck dura Brand of Potassium Iodide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Merck dura Brand of Potassium Iodide 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 Merck dura Brand of Potassium Iodide supplier is an individual or a company that provides Merck dura Brand of Potassium Iodide active pharmaceutical ingredient (API) or Merck dura Brand of Potassium Iodide finished formulations upon request. The Merck dura Brand of Potassium Iodide suppliers may include Merck dura Brand of Potassium Iodide API manufacturers, exporters, distributors and traders.
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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 Merck dura Brand of Potassium Iodide Drug Master File in Japan (Merck dura Brand of Potassium Iodide JDMF) empowers Merck dura Brand of Potassium Iodide 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 Merck dura Brand of Potassium Iodide JDMF during the approval evaluation for pharmaceutical products. At the time of Merck dura Brand of Potassium Iodide 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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