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 only)
Registration Number : 218MF10329
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2017-07-31
A Droperidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Droperidol, including repackagers and relabelers. The FDA regulates Droperidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Droperidol 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 Droperidol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Droperidol supplier is an individual or a company that provides Droperidol active pharmaceutical ingredient (API) or Droperidol finished formulations upon request. The Droperidol suppliers may include Droperidol API manufacturers, exporters, distributors and traders.
click here to find a list of Droperidol 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 Droperidol Drug Master File in Japan (Droperidol JDMF) empowers Droperidol 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 Droperidol JDMF during the approval evaluation for pharmaceutical products. At the time of Droperidol 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 Droperidol suppliers with JDMF on PharmaCompass.
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