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
A Hexahydrothymol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexahydrothymol, including repackagers and relabelers. The FDA regulates Hexahydrothymol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexahydrothymol 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 Hexahydrothymol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hexahydrothymol supplier is an individual or a company that provides Hexahydrothymol active pharmaceutical ingredient (API) or Hexahydrothymol finished formulations upon request. The Hexahydrothymol suppliers may include Hexahydrothymol API manufacturers, exporters, distributors and traders.
click here to find a list of Hexahydrothymol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hexahydrothymol CEP of the European Pharmacopoeia monograph is often referred to as a Hexahydrothymol Certificate of Suitability (COS). The purpose of a Hexahydrothymol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hexahydrothymol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hexahydrothymol to their clients by showing that a Hexahydrothymol CEP has been issued for it. The manufacturer submits a Hexahydrothymol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hexahydrothymol CEP holder for the record. Additionally, the data presented in the Hexahydrothymol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hexahydrothymol DMF.
A Hexahydrothymol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hexahydrothymol 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 Hexahydrothymol suppliers with CEP (COS) on PharmaCompass.
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