01 2Kanto Chemical Co., Ltd.
01 1Potassium hydroxide
02 1Potassium hydroxide (UE-E)
01 2Japan
Registration Number : 219MF10218
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-07-06
Latest Date of Registration : 2007-07-06
Registration Number : 219MF10060
Registrant's Address : 3-2-8 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2007-03-05
Latest Date of Registration : 2007-03-05
A Potassium Hydroxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Potassium Hydroxide, including repackagers and relabelers. The FDA regulates Potassium Hydroxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Potassium Hydroxide 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 Potassium Hydroxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Potassium Hydroxide supplier is an individual or a company that provides Potassium Hydroxide active pharmaceutical ingredient (API) or Potassium Hydroxide finished formulations upon request. The Potassium Hydroxide suppliers may include Potassium Hydroxide API manufacturers, exporters, distributors and traders.
click here to find a list of Potassium Hydroxide 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 Potassium Hydroxide Drug Master File in Japan (Potassium Hydroxide JDMF) empowers Potassium Hydroxide 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 Potassium Hydroxide JDMF during the approval evaluation for pharmaceutical products. At the time of Potassium Hydroxide 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 Potassium Hydroxide suppliers with JDMF on PharmaCompass.
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