01 1BASF SE Ludwigshafen DE
02 1FREY + LAU GMBH Henstedt-Ulzburg DE
03 1JINDAL DRUGS PVT. LTD. Taloja IN
04 1SYMRISE AG Holzminden DE
01 3Levomenthol
02 1Levomenthol, Flakes and solid mass
01 3Germany
02 1India
01 4Valid
Levomenthol, Flakes And Solid Mass
Certificate Number : R1-CEP 2012-390 - Rev 01
Status : Valid
Issue Date : 2021-06-16
Type : Chemical
Substance Number : 619
Certificate Number : R0-CEP 2019-058 - Rev 00
Status : Valid
Issue Date : 2021-01-25
Type : Chemical
Substance Number : 619
Certificate Number : R0-CEP 2018-211 - Rev 00
Status : Valid
Issue Date : 2021-04-01
Type : Chemical
Substance Number : 619
Certificate Number : R1-CEP 2004-100 - Rev 03
Status : Valid
Issue Date : 2020-04-21
Type : Chemical
Substance Number : 619
98
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 I-menthol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of I-menthol, including repackagers and relabelers. The FDA regulates I-menthol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. I-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 I-menthol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A I-menthol supplier is an individual or a company that provides I-menthol active pharmaceutical ingredient (API) or I-menthol finished formulations upon request. The I-menthol suppliers may include I-menthol API manufacturers, exporters, distributors and traders.
click here to find a list of I-menthol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A I-menthol CEP of the European Pharmacopoeia monograph is often referred to as a I-menthol Certificate of Suitability (COS). The purpose of a I-menthol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of I-menthol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of I-menthol to their clients by showing that a I-menthol CEP has been issued for it. The manufacturer submits a I-menthol CEP (COS) as part of the market authorization procedure, and it takes on the role of a I-menthol CEP holder for the record. Additionally, the data presented in the I-menthol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the I-menthol DMF.
A I-menthol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. I-menthol CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of I-menthol suppliers with CEP (COS) on PharmaCompass.
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