01 1DYNAMIT NOBEL GmbH
02 1Toyo Pharmaceutical Co., Ltd.
01 140% mandelic nitrile ethanol solution
02 15% nitroglycerin-ethanol solution
01 1Germany
02 1Japan
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 : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 2-1-5
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethanol manufacturer or Ethanol supplier.
PharmaCompass also assists you with knowing the Ethanol API Price utilized in the formulation of products. Ethanol API Price is not always fixed or binding as the Ethanol Price is obtained through a variety of data sources. The Ethanol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ethyl alcohol, undenatured manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethyl alcohol, undenatured, including repackagers and relabelers. The FDA regulates Ethyl alcohol, undenatured manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethyl alcohol, undenatured 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 Ethyl alcohol, undenatured supplier is an individual or a company that provides Ethyl alcohol, undenatured active pharmaceutical ingredient (API) or Ethyl alcohol, undenatured finished formulations upon request. The Ethyl alcohol, undenatured suppliers may include Ethyl alcohol, undenatured API manufacturers, exporters, distributors and traders.
click here to find a list of Ethyl alcohol, undenatured 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 Ethyl alcohol, undenatured Drug Master File in Japan (Ethyl alcohol, undenatured JDMF) empowers Ethyl alcohol, undenatured 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 Ethyl alcohol, undenatured JDMF during the approval evaluation for pharmaceutical products. At the time of Ethyl alcohol, undenatured 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 Ethyl alcohol, undenatured suppliers with JDMF on PharmaCompass.
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