01 1DOTTIKON EXCLUSIVE SYNTHESIS AG
02 2Dipharma Francis Srl
01 1ISOSORBIDE DINITRATE, DILUTED
02 2Isosorbide Dinitrate
01 2Italy
02 1Switzerland
NDC Package Code : 46438-0001
Start Marketing Date : 2005-08-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0634
Start Marketing Date : 2013-08-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54864-106
Start Marketing Date : 1983-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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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 Cedocard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cedocard, including repackagers and relabelers. The FDA regulates Cedocard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cedocard 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 Cedocard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cedocard supplier is an individual or a company that provides Cedocard active pharmaceutical ingredient (API) or Cedocard finished formulations upon request. The Cedocard suppliers may include Cedocard API manufacturers, exporters, distributors and traders.
click here to find a list of Cedocard suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Cedocard as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cedocard API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Cedocard as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Cedocard and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cedocard NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cedocard suppliers with NDC on PharmaCompass.
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