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
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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.
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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 Tox21_202608 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202608, including repackagers and relabelers. The FDA regulates Tox21_202608 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202608 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tox21_202608 supplier is an individual or a company that provides Tox21_202608 active pharmaceutical ingredient (API) or Tox21_202608 finished formulations upon request. The Tox21_202608 suppliers may include Tox21_202608 API manufacturers, exporters, distributors and traders.
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A Tox21_202608 CEP of the European Pharmacopoeia monograph is often referred to as a Tox21_202608 Certificate of Suitability (COS). The purpose of a Tox21_202608 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tox21_202608 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tox21_202608 to their clients by showing that a Tox21_202608 CEP has been issued for it. The manufacturer submits a Tox21_202608 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tox21_202608 CEP holder for the record. Additionally, the data presented in the Tox21_202608 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tox21_202608 DMF.
A Tox21_202608 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tox21_202608 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 4 companies offering Tox21_202608
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