01 1Joint Stock Company Grindeks
02 1Yoshindo Holdings 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
Japanese Pharmacopoeia Droperidol (for manufacturing purposes only)
Registration Number : 218MF10329
Registrant's Address : 3697-8 Hagishima, Fuchu-machi, 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, and more, enabling you to easily find the right Droperidol manufacturer or Droperidol supplier for your needs.
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A Inopsin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Inopsin, including repackagers and relabelers. The FDA regulates Inopsin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Inopsin 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 Inopsin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Inopsin supplier is an individual or a company that provides Inopsin active pharmaceutical ingredient (API) or Inopsin finished formulations upon request. The Inopsin suppliers may include Inopsin API manufacturers, exporters, distributors and traders.
click here to find a list of Inopsin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Inopsin Drug Master File in Japan (Inopsin JDMF) empowers Inopsin 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 Inopsin JDMF during the approval evaluation for pharmaceutical products. At the time of Inopsin 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 Inopsin suppliers with JDMF on PharmaCompass.
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