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.
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 Denatured alcohol SD-39c manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Denatured alcohol SD-39c, including repackagers and relabelers. The FDA regulates Denatured alcohol SD-39c manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Denatured alcohol SD-39c 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 Denatured alcohol SD-39c manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Denatured alcohol SD-39c supplier is an individual or a company that provides Denatured alcohol SD-39c active pharmaceutical ingredient (API) or Denatured alcohol SD-39c finished formulations upon request. The Denatured alcohol SD-39c suppliers may include Denatured alcohol SD-39c API manufacturers, exporters, distributors and traders.
click here to find a list of Denatured alcohol SD-39c 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 Denatured alcohol SD-39c Drug Master File in Japan (Denatured alcohol SD-39c JDMF) empowers Denatured alcohol SD-39c 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 Denatured alcohol SD-39c JDMF during the approval evaluation for pharmaceutical products. At the time of Denatured alcohol SD-39c 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 Denatured alcohol SD-39c suppliers with JDMF on PharmaCompass.
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