01 1Ace Japan Co., Ltd.
02 1CENTIP HARM
03 1UBE Inc.
01 1Japanese Pharmacopoeia Levomepromazine maleate
02 1Levomepromazine
03 1Rebotomin
01 1France
02 2Japan
Japanese Pharmacopoeia Levomepromazine Maleate
Registration Number : 218MF10956
Registrant's Address : 5850-1 Higashine-ko, Higashine City, Yamagata Prefecture
Initial Date of Registration : 2006-11-24
Latest Date of Registration : 2006-11-24
Registration Number : 217MF10891
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2005-11-07
Latest Date of Registration : 2019-05-08
Registration Number : 228MF10182
Registrant's Address : Chemin de la Madeleine 06130 GRASSE FRANCE
Initial Date of Registration : 2016-09-08
Latest Date of Registration : 2019-04-22
A Levomepromazine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levomepromazine Maleate, including repackagers and relabelers. The FDA regulates Levomepromazine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levomepromazine Maleate 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 Levomepromazine Maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levomepromazine Maleate supplier is an individual or a company that provides Levomepromazine Maleate active pharmaceutical ingredient (API) or Levomepromazine Maleate finished formulations upon request. The Levomepromazine Maleate suppliers may include Levomepromazine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Levomepromazine Maleate 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 Levomepromazine Maleate Drug Master File in Japan (Levomepromazine Maleate JDMF) empowers Levomepromazine Maleate 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 Levomepromazine Maleate JDMF during the approval evaluation for pharmaceutical products. At the time of Levomepromazine Maleate 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 Levomepromazine Maleate suppliers with JDMF on PharmaCompass.
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