01 2Tsujimoto Chemical Industry Co., Ltd.
01 1Methylenedioxy salicylic acid promethazine
02 1Promethazine methylene di salicylate
01 2Japan
Promethazine methylenedisalicylate
Registration Number : 217MF11311
Registrant's Address : Osaka Prefecture, Osaka City, Tsurumi Ward, Tsurumi 1-6-88
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2006-04-07
Promethazine methylene disalicylate
Registration Number : 219MF10270
Registrant's Address : Osaka Prefecture, Osaka City, Tsurumi Ward, Tsurumi 1-6-93
Initial Date of Registration : 2007-08-16
Latest Date of Registration : 2009-06-30
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PharmaCompass offers a list of Promethazine 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 Promethazine manufacturer or Promethazine supplier for your needs.
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PharmaCompass also assists you with knowing the Promethazine API Price utilized in the formulation of products. Promethazine API Price is not always fixed or binding as the Promethazine Price is obtained through a variety of data sources. The Promethazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lergigan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lergigan, including repackagers and relabelers. The FDA regulates Lergigan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lergigan 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 Lergigan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lergigan supplier is an individual or a company that provides Lergigan active pharmaceutical ingredient (API) or Lergigan finished formulations upon request. The Lergigan suppliers may include Lergigan API manufacturers, exporters, distributors and traders.
click here to find a list of Lergigan 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 Lergigan Drug Master File in Japan (Lergigan JDMF) empowers Lergigan 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 Lergigan JDMF during the approval evaluation for pharmaceutical products. At the time of Lergigan 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 Lergigan suppliers with JDMF on PharmaCompass.
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