01 1DYNAMIT NOBEL GmbH
02 1Toyo Pharmaceutical Chemical Co., Ltd.
01 140% mandelic nitrile ethanol solution
02 15% nitroglycerin-ethanol solution
01 1Germany
02 1Japan
5% nitroglycerin ethanol solution
Registration Number : 218MF10624
Registrant's Address : Kalkstrasse 218, 51377 Leverkusen, Germany
Initial Date of Registration : 2006-07-20
Latest Date of Registration : 2020-12-15
40% Mandelnitrile Ethanol Solution
Registration Number : 218MF10694
Registrant's Address : 2-1-5 Doshomachi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2006-08-11
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PharmaCompass offers a list of Ethanol 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 Ethanol manufacturer or Ethanol supplier for your needs.
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A UNII-3K9958V90M manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-3K9958V90M, including repackagers and relabelers. The FDA regulates UNII-3K9958V90M manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-3K9958V90M 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 UNII-3K9958V90M supplier is an individual or a company that provides UNII-3K9958V90M active pharmaceutical ingredient (API) or UNII-3K9958V90M finished formulations upon request. The UNII-3K9958V90M suppliers may include UNII-3K9958V90M 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 UNII-3K9958V90M Drug Master File in Japan (UNII-3K9958V90M JDMF) empowers UNII-3K9958V90M 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 UNII-3K9958V90M JDMF during the approval evaluation for pharmaceutical products. At the time of UNII-3K9958V90M 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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