01 1Bussan Food Science Co., Ltd.
02 1Mitsubishi Corporation Life Sciences Ltd.
01 1Japanese Pharmacopoeia xylitol
02 1Xylitol
01 2Japan
Japanese Pharmacopoeia Xylitol
Registration Number : 218MF10313
Registrant's Address : 24-12 Kitahama-cho, Chita City, Aichi Prefecture
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2006-02-28
Registration Number : 217MF10326
Registrant's Address : 1-1-3 Yurakucho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-07-14
Latest Date of Registration : 2006-03-24
A Ribitol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ribitol, including repackagers and relabelers. The FDA regulates Ribitol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ribitol 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 Ribitol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ribitol supplier is an individual or a company that provides Ribitol active pharmaceutical ingredient (API) or Ribitol finished formulations upon request. The Ribitol suppliers may include Ribitol API manufacturers, exporters, distributors and traders.
click here to find a list of Ribitol 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 Ribitol Drug Master File in Japan (Ribitol JDMF) empowers Ribitol 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 Ribitol JDMF during the approval evaluation for pharmaceutical products. At the time of Ribitol 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 Ribitol suppliers with JDMF on PharmaCompass.
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