01 1BASF SE
02 2Suzuki Mint Co., Ltd.
01 1Hakkano
02 1Menthol brain
03 1l-menthol L-menthol
01 2Japan
02 1Blank
Registration Number : 231MF10076
Registrant's Address : Carl-Bosch-Strasse 38,67056 Ludwigshafen, Federal Republic of Germany
Initial Date of Registration : 2019-03-19
Latest Date of Registration : 2021-10-13
Registration Number : 230MF10155
Registrant's Address : Hyogo Prefecture Kobe City Chuo Ward Minatojima Minamimachi 3-2-12
Initial Date of Registration : 2018-11-14
Latest Date of Registration : 2018-11-14
Registration Number : 218MF10570
Registrant's Address : 1-3-1 Shimokawahara-dori, Nada-ku, Kobe City, Hyogo Prefecture
Initial Date of Registration : 2006-06-15
Latest Date of Registration : 2010-07-09
A Menthol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Menthol, including repackagers and relabelers. The FDA regulates Menthol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Menthol 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 Menthol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Menthol supplier is an individual or a company that provides Menthol active pharmaceutical ingredient (API) or Menthol finished formulations upon request. The Menthol suppliers may include Menthol API manufacturers, exporters, distributors and traders.
click here to find a list of Menthol 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 Menthol Drug Master File in Japan (Menthol JDMF) empowers Menthol 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 Menthol JDMF during the approval evaluation for pharmaceutical products. At the time of Menthol 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 Menthol suppliers with JDMF on PharmaCompass.
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