01 1SperaNexus Inc.
02 1Yamamoto Chemical Industry Co., Ltd.
01 1Salicylamide
02 1Salicylamide "Iwaki"
01 2Japan
Registration Number : 217MF10052
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration : 2007-09-18
Registration Number : 221MF10163
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2009-07-23
Latest Date of Registration : 2009-07-23
A Salicylamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salicylamide, including repackagers and relabelers. The FDA regulates Salicylamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salicylamide 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 Salicylamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Salicylamide supplier is an individual or a company that provides Salicylamide active pharmaceutical ingredient (API) or Salicylamide finished formulations upon request. The Salicylamide suppliers may include Salicylamide API manufacturers, exporters, distributors and traders.
click here to find a list of Salicylamide 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 Salicylamide Drug Master File in Japan (Salicylamide JDMF) empowers Salicylamide 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 Salicylamide JDMF during the approval evaluation for pharmaceutical products. At the time of Salicylamide 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 Salicylamide suppliers with JDMF on PharmaCompass.
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