01 1Joint Stock Company Grindeks
02 1Yoshindo Co., Ltd.
01 1Day stations droperidol (production only)
02 1Droperidol
01 1Japan
02 1Latvia
Registration Number : 220MF10090
Registrant's Address : 53 Krustpils Street, Riga, Latvia
Initial Date of Registration : 2008-03-28
Latest Date of Registration : 2019-12-25
Droperidol (JP) (for manufacturing purposes only)
Registration Number : 218MF10329
Registrant's Address : 3697-8 Hagishima, Funamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2017-07-31
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PharmaCompass offers a list of Droperidol 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 Droperidol manufacturer or Droperidol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Droperidol manufacturer or Droperidol supplier.
PharmaCompass also assists you with knowing the Droperidol API Price utilized in the formulation of products. Droperidol API Price is not always fixed or binding as the Droperidol Price is obtained through a variety of data sources. The Droperidol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dropel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dropel, including repackagers and relabelers. The FDA regulates Dropel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dropel 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 Dropel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dropel supplier is an individual or a company that provides Dropel active pharmaceutical ingredient (API) or Dropel finished formulations upon request. The Dropel suppliers may include Dropel API manufacturers, exporters, distributors and traders.
click here to find a list of Dropel 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 Dropel Drug Master File in Japan (Dropel JDMF) empowers Dropel 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 Dropel JDMF during the approval evaluation for pharmaceutical products. At the time of Dropel 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 Dropel suppliers with JDMF on PharmaCompass.
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