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01 2DIPHARMA FRANCIS S.R.L. Baranzate IT
02 1EIRCHEM PHARMA SERVICES LIMITED Shannon IE
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01 1Isosorbide dinitrate, diluted
02 1Isosorbide dinitrate, diluted, 25% in lactose monohydrate
03 1Isosorbide dinitrate, diluted, 40% in lactose monohydrate
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01 1Ireland
02 2Italy
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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Status : Withdrawn by EDQM Failure to CEP pro...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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isosorbide Dinitrate manufacturer or Isosorbide Dinitrate supplier.
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 Cardio 10 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cardio 10, including repackagers and relabelers. The FDA regulates Cardio 10 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cardio 10 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 Cardio 10 supplier is an individual or a company that provides Cardio 10 active pharmaceutical ingredient (API) or Cardio 10 finished formulations upon request. The Cardio 10 suppliers may include Cardio 10 API manufacturers, exporters, distributors and traders.
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A Cardio 10 CEP of the European Pharmacopoeia monograph is often referred to as a Cardio 10 Certificate of Suitability (COS). The purpose of a Cardio 10 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cardio 10 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cardio 10 to their clients by showing that a Cardio 10 CEP has been issued for it. The manufacturer submits a Cardio 10 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cardio 10 CEP holder for the record. Additionally, the data presented in the Cardio 10 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cardio 10 DMF.
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