01 1SperaNexus Inc.
01 1Tartaric acid ifenprodil
01 1Japan
Registration Number : 217MF10041
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2009-12-25
A Ifenprodil Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ifenprodil Tartrate, including repackagers and relabelers. The FDA regulates Ifenprodil Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ifenprodil Tartrate 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 Ifenprodil Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ifenprodil Tartrate supplier is an individual or a company that provides Ifenprodil Tartrate active pharmaceutical ingredient (API) or Ifenprodil Tartrate finished formulations upon request. The Ifenprodil Tartrate suppliers may include Ifenprodil Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Ifenprodil Tartrate 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 Ifenprodil Tartrate Drug Master File in Japan (Ifenprodil Tartrate JDMF) empowers Ifenprodil Tartrate 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 Ifenprodil Tartrate JDMF during the approval evaluation for pharmaceutical products. At the time of Ifenprodil Tartrate 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 Ifenprodil Tartrate suppliers with JDMF on PharmaCompass.
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