Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1IPCA Laboratories Limited Mumbai IN
01 2Triamterene
01 1India
02 1Spain
01 2Valid
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : R1-CEP 1996-038 - Rev 04
Status : Valid
Issue Date : 2018-10-09
Type : Chemical
Substance Number : 58
Certificate Number : R1-CEP 2011-203 - Rev 00
Status : Valid
Issue Date : 2017-09-29
Type : Chemical
Substance Number : 58
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PharmaCompass offers a list of Triamterene 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 Triamterene manufacturer or Triamterene supplier for your needs.
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PharmaCompass also assists you with knowing the Triamterene API Price utilized in the formulation of products. Triamterene API Price is not always fixed or binding as the Triamterene Price is obtained through a variety of data sources. The Triamterene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dyrenium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dyrenium, including repackagers and relabelers. The FDA regulates Dyrenium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dyrenium 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 Dyrenium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dyrenium supplier is an individual or a company that provides Dyrenium active pharmaceutical ingredient (API) or Dyrenium finished formulations upon request. The Dyrenium suppliers may include Dyrenium API manufacturers, exporters, distributors and traders.
click here to find a list of Dyrenium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dyrenium CEP of the European Pharmacopoeia monograph is often referred to as a Dyrenium Certificate of Suitability (COS). The purpose of a Dyrenium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dyrenium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dyrenium to their clients by showing that a Dyrenium CEP has been issued for it. The manufacturer submits a Dyrenium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dyrenium CEP holder for the record. Additionally, the data presented in the Dyrenium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dyrenium DMF.
A Dyrenium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dyrenium 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 Dyrenium suppliers with CEP (COS) on PharmaCompass.
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