01 1CHIERON ACTIVE INGREDIENTS PRIVATE LIMITED Hyderabad IN
02 1SIEGFRIED EVIONNAZ SA Evionnaz CH
01 2Tetracaine hydrochloride
01 1Switzerland
02 1Blank
01 2Valid
Certificate Number : CEP 2017-205 - Rev 01
Status : Valid
Issue Date : 2024-01-29
Type : Chemical
Substance Number : 57
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Certificate Number : CEP 2010-256 - Rev 02
Status : Valid
Issue Date : 2025-06-17
Type : Chemical
Substance Number : 57
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PharmaCompass offers a list of Tetracaine Hydrochloride 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 Tetracaine Hydrochloride manufacturer or Tetracaine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Tetracaine Hydrochloride API Price utilized in the formulation of products. Tetracaine Hydrochloride API Price is not always fixed or binding as the Tetracaine Hydrochloride Price is obtained through a variety of data sources. The Tetracaine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tonexol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tonexol, including repackagers and relabelers. The FDA regulates Tonexol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tonexol 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 Tonexol supplier is an individual or a company that provides Tonexol active pharmaceutical ingredient (API) or Tonexol finished formulations upon request. The Tonexol suppliers may include Tonexol API manufacturers, exporters, distributors and traders.
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A Tonexol CEP of the European Pharmacopoeia monograph is often referred to as a Tonexol Certificate of Suitability (COS). The purpose of a Tonexol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tonexol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tonexol to their clients by showing that a Tonexol CEP has been issued for it. The manufacturer submits a Tonexol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tonexol CEP holder for the record. Additionally, the data presented in the Tonexol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tonexol DMF.
A Tonexol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tonexol 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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