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
A Triamterene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triamterene, including repackagers and relabelers. The FDA regulates Triamterene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triamterene 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 Triamterene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triamterene supplier is an individual or a company that provides Triamterene active pharmaceutical ingredient (API) or Triamterene finished formulations upon request. The Triamterene suppliers may include Triamterene API manufacturers, exporters, distributors and traders.
click here to find a list of Triamterene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Triamterene CEP of the European Pharmacopoeia monograph is often referred to as a Triamterene Certificate of Suitability (COS). The purpose of a Triamterene CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Triamterene EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Triamterene to their clients by showing that a Triamterene CEP has been issued for it. The manufacturer submits a Triamterene CEP (COS) as part of the market authorization procedure, and it takes on the role of a Triamterene CEP holder for the record. Additionally, the data presented in the Triamterene CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Triamterene DMF.
A Triamterene CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Triamterene 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 Triamterene suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Triamterene
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
