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