01 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
02 1Shiono Finesse Co., Ltd.
01 1Bromperidol
02 1Bromperidol For manufacturing only
01 2Japan
Bromperidol For manufacturing purposes only
Registration Number : 305MF10052
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2023-04-25
Latest Date of Registration : 2023-04-25
Registration Number : 220MF10075
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 3-1-6
Initial Date of Registration : 2008-03-14
Latest Date of Registration : 2008-03-14
A Bromperidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bromperidol, including repackagers and relabelers. The FDA regulates Bromperidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bromperidol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Bromperidol supplier is an individual or a company that provides Bromperidol active pharmaceutical ingredient (API) or Bromperidol finished formulations upon request. The Bromperidol suppliers may include Bromperidol API manufacturers, exporters, distributors and traders.
click here to find a list of Bromperidol 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 Bromperidol Drug Master File in Japan (Bromperidol JDMF) empowers Bromperidol 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 Bromperidol JDMF during the approval evaluation for pharmaceutical products. At the time of Bromperidol 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 Bromperidol suppliers with JDMF on PharmaCompass.
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