01 1Active Pharma Inc.
02 1Daito Co., Ltd.
03 1Permakem Asia Co., Ltd.
01 3Nilvadipine
01 3Japan
Registration Number : 217MF10658
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-09-29
Latest Date of Registration : 2006-08-23
Registration Number : 217MF10720
Registrant's Address : 7-6, Nihonbashi Odenmacho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2008-02-08
Registration Number : 218MF10356
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2018-10-01
A Nilvadipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nilvadipine, including repackagers and relabelers. The FDA regulates Nilvadipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nilvadipine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Nilvadipine supplier is an individual or a company that provides Nilvadipine active pharmaceutical ingredient (API) or Nilvadipine finished formulations upon request. The Nilvadipine suppliers may include Nilvadipine API manufacturers, exporters, distributors and traders.
click here to find a list of Nilvadipine 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 Nilvadipine Drug Master File in Japan (Nilvadipine JDMF) empowers Nilvadipine 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 Nilvadipine JDMF during the approval evaluation for pharmaceutical products. At the time of Nilvadipine 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 Nilvadipine suppliers with JDMF on PharmaCompass.
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