01 1Alps Pharmaceutical Co., Ltd.
02 1DSM Nutritional Products Ltd.
01 1Panthenol
02 1Panthenol D-Panthenol
01 1Japan
02 1Netherlands
Registration Number : 217MF11027
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2005-12-02
Latest Date of Registration : 2008-12-04
Registration Number : 217MF11287
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2006-07-20
A D-Panthenol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D-Panthenol, including repackagers and relabelers. The FDA regulates D-Panthenol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D-Panthenol 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 D-Panthenol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A D-Panthenol supplier is an individual or a company that provides D-Panthenol active pharmaceutical ingredient (API) or D-Panthenol finished formulations upon request. The D-Panthenol suppliers may include D-Panthenol API manufacturers, exporters, distributors and traders.
click here to find a list of D-Panthenol 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 D-Panthenol Drug Master File in Japan (D-Panthenol JDMF) empowers D-Panthenol 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 D-Panthenol JDMF during the approval evaluation for pharmaceutical products. At the time of D-Panthenol 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 D-Panthenol suppliers with JDMF on PharmaCompass.
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