01 2DIPHARMA FRANCIS S.R.L. Baranzate IT
02 1EIRCHEM PHARMA SERVICES LIMITED Shannon IE
01 1Isosorbide dinitrate, diluted
02 1Isosorbide dinitrate, diluted, 25% in lactose monohydrate
03 1Isosorbide dinitrate, diluted, 40% in lactose monohydrate
01 1Ireland
02 2Italy
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
Isosorbide Dinitrate, Diluted, 25% In Lactose Mo...
Certificate Number : R1-CEP 2013-295 - Rev 00
Status : Valid
Issue Date : 2022-02-09
Type : Chemical
Substance Number : 1117
Isosorbide Dinitrate, Diluted, 40% In Lactose Mo...
Certificate Number : R1-CEP 2013-298 - Rev 00
Status : Valid
Issue Date : 2022-02-09
Type : Chemical
Substance Number : 1117
Certificate Number : R1-CEP 1998-133 - Rev 05
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2019-11-26
Type : Chemical
Substance Number : 1117
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PharmaCompass offers a list of Isosorbide Dinitrate 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 Isosorbide Dinitrate manufacturer or Isosorbide Dinitrate supplier for your needs.
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PharmaCompass also assists you with knowing the Isosorbide Dinitrate API Price utilized in the formulation of products. Isosorbide Dinitrate API Price is not always fixed or binding as the Isosorbide Dinitrate Price is obtained through a variety of data sources. The Isosorbide Dinitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cardonit 40 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cardonit 40, including repackagers and relabelers. The FDA regulates Cardonit 40 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cardonit 40 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 Cardonit 40 supplier is an individual or a company that provides Cardonit 40 active pharmaceutical ingredient (API) or Cardonit 40 finished formulations upon request. The Cardonit 40 suppliers may include Cardonit 40 API manufacturers, exporters, distributors and traders.
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A Cardonit 40 CEP of the European Pharmacopoeia monograph is often referred to as a Cardonit 40 Certificate of Suitability (COS). The purpose of a Cardonit 40 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cardonit 40 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cardonit 40 to their clients by showing that a Cardonit 40 CEP has been issued for it. The manufacturer submits a Cardonit 40 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cardonit 40 CEP holder for the record. Additionally, the data presented in the Cardonit 40 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cardonit 40 DMF.
A Cardonit 40 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cardonit 40 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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