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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 Levomenthol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levomenthol, including repackagers and relabelers. The FDA regulates Levomenthol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levomenthol 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 Levomenthol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levomenthol supplier is an individual or a company that provides Levomenthol active pharmaceutical ingredient (API) or Levomenthol finished formulations upon request. The Levomenthol suppliers may include Levomenthol API manufacturers, exporters, distributors and traders.
click here to find a list of Levomenthol 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 Levomenthol Drug Master File in Japan (Levomenthol JDMF) empowers Levomenthol 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 Levomenthol JDMF during the approval evaluation for pharmaceutical products. At the time of Levomenthol 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 Levomenthol suppliers with JDMF on PharmaCompass.
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