01 1Ace Japan Co., Ltd.
02 1Katsura Chemical Co., Ltd.
01 2Periciazine
01 2Japan
Registration Number : 217MF10136
Registrant's Address : Yamagata Prefecture Higashine City Higashine City 5850-1
Initial Date of Registration : 2005-05-24
Latest Date of Registration : 2006-06-09
Registration Number : 220MF10200
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2008-09-19
Latest Date of Registration : 2008-09-19
A propericiazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of propericiazine, including repackagers and relabelers. The FDA regulates propericiazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. propericiazine 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 propericiazine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A propericiazine supplier is an individual or a company that provides propericiazine active pharmaceutical ingredient (API) or propericiazine finished formulations upon request. The propericiazine suppliers may include propericiazine API manufacturers, exporters, distributors and traders.
click here to find a list of propericiazine 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 propericiazine Drug Master File in Japan (propericiazine JDMF) empowers propericiazine 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 propericiazine JDMF during the approval evaluation for pharmaceutical products. At the time of propericiazine 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 propericiazine suppliers with JDMF on PharmaCompass.
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