01 1Nagaoka Jitsugyo Co., Ltd.
02 1Ogi Pharmaceutical Co., Ltd.
03 1Symrise AG
04 1Takasago International Corporation
05 2Toyo Mint Industry Co., Ltd.
01 2Japanese Pharmacopoeia l- menthol (production only)
02 1Menthol JP
03 2l- menthol
04 1l- menthol SL-21
01 1Germany
02 5Japan
Japanese Pharmacopoeia l-Menthol (for manufacturing only)
Registration Number : 218MF10275
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 2-5-8
Initial Date of Registration : 2006-02-23
Latest Date of Registration : 2006-02-23
Japanese Pharmacopoeia l-Menthol (for manufacturing only)
Registration Number : 217MF10801
Registrant's Address : Hyogo Prefecture Nishinomiya City Nishinomiyahama 4-7-18
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2006-11-15
Registration Number : 218MF10705
Registrant's Address : Muehlenfeldstrasse 1 D-37 603 Holzminden Germany
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2013-05-09
Registration Number : 217MF11171
Registrant's Address : 5-37-1 Kamata, Ota-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-04-01
Registration Number : 217MF10175
Registrant's Address : 75-1 Hamanaka, Satosho-cho, Asakuchi-gun, Okayama Prefecture
Initial Date of Registration : 2005-05-31
Latest Date of Registration : 2006-11-15
Registration Number : 217MF10179
Registrant's Address : 75-1 Hamanaka, Satosho-cho, Asakuchi-gun, Okayama Prefecture
Initial Date of Registration : 2005-05-31
Latest Date of Registration : 2007-03-14
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PharmaCompass offers a list of Levomenthol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Levomenthol manufacturer or Levomenthol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levomenthol manufacturer or Levomenthol supplier.
PharmaCompass also assists you with knowing the Levomenthol API Price utilized in the formulation of products. Levomenthol API Price is not always fixed or binding as the Levomenthol Price is obtained through a variety of data sources. The Levomenthol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A L-MENTHOL USP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-MENTHOL USP, including repackagers and relabelers. The FDA regulates L-MENTHOL USP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-MENTHOL USP 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 L-MENTHOL USP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A L-MENTHOL USP supplier is an individual or a company that provides L-MENTHOL USP active pharmaceutical ingredient (API) or L-MENTHOL USP finished formulations upon request. The L-MENTHOL USP suppliers may include L-MENTHOL USP API manufacturers, exporters, distributors and traders.
click here to find a list of L-MENTHOL USP 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 L-MENTHOL USP Drug Master File in Japan (L-MENTHOL USP JDMF) empowers L-MENTHOL USP 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 L-MENTHOL USP JDMF during the approval evaluation for pharmaceutical products. At the time of L-MENTHOL USP 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 L-MENTHOL USP suppliers with JDMF on PharmaCompass.
We have 5 companies offering L-MENTHOL USP
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