01 1Ace Japan Co., Ltd.
02 1CENTIP HARM
03 1UBE Co., Ltd.
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
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PharmaCompass offers a list of Levomepromazine Maleate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Levomepromazine Maleate manufacturer or Levomepromazine Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levomepromazine Maleate manufacturer or Levomepromazine Maleate supplier.
PharmaCompass also assists you with knowing the Levomepromazine Maleate API Price utilized in the formulation of products. Levomepromazine Maleate API Price is not always fixed or binding as the Levomepromazine Maleate Price is obtained through a variety of data sources. The Levomepromazine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levomepromazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levomepromazine, including repackagers and relabelers. The FDA regulates Levomepromazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levomepromazine 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levomepromazine supplier is an individual or a company that provides Levomepromazine active pharmaceutical ingredient (API) or Levomepromazine finished formulations upon request. The Levomepromazine suppliers may include Levomepromazine API manufacturers, exporters, distributors and traders.
click here to find a list of Levomepromazine 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 Drug Master File in Japan (Levomepromazine JDMF) empowers Levomepromazine 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Levomepromazine 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 suppliers with JDMF on PharmaCompass.
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