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