01 2CHANGZHOU YABANG PHARMACEUTICAL CO. , LTD.
02 1SperaNexus Co., Ltd.
01 1MEXILETINE HYDROCHLORIDE
02 2Mexiletine hydrochloride
01 2China
02 1Japan
Registration Number : 230MF10140
Registrant's Address : Liangchang East Road 6#, Jintan, Jiangsu Province, P. R. China
Initial Date of Registration : 2018-10-12
Latest Date of Registration : 2018-10-12
Registration Number : 220MF10055
Registrant's Address : Liangchang East Road 6#, Jintan, Jiangsu Province, P. R. China
Initial Date of Registration : 2008-02-08
Latest Date of Registration : 2010-07-26
Registration Number : 217MF10039
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2010-02-09
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PharmaCompass offers a list of Mexiletine 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 Mexiletine manufacturer or Mexiletine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mexiletine manufacturer or Mexiletine supplier.
PharmaCompass also assists you with knowing the Mexiletine API Price utilized in the formulation of products. Mexiletine API Price is not always fixed or binding as the Mexiletine Price is obtained through a variety of data sources. The Mexiletine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ritalmex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritalmex, including repackagers and relabelers. The FDA regulates Ritalmex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritalmex 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 Ritalmex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ritalmex supplier is an individual or a company that provides Ritalmex active pharmaceutical ingredient (API) or Ritalmex finished formulations upon request. The Ritalmex suppliers may include Ritalmex API manufacturers, exporters, distributors and traders.
click here to find a list of Ritalmex 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 Ritalmex Drug Master File in Japan (Ritalmex JDMF) empowers Ritalmex 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 Ritalmex JDMF during the approval evaluation for pharmaceutical products. At the time of Ritalmex 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 Ritalmex suppliers with JDMF on PharmaCompass.
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