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Isosorbide Dinitrate - 54569-0452-0 - (Isosorbide Dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 54569-0452
Proprietary Name: Isosorbide Dinitrate
Non Proprietary Name: Isosorbide Dinitrate
Active Ingredient(s): 20    mg/1 & nbsp;   Isosorbide Dinitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Isosorbide Dinitrate

Product NDC: 54569-0452
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089367
Marketing Category: ANDA
Start Marketing Date: 19880407

Package Information of Isosorbide Dinitrate

Package NDC: 54569-0452-0
Package Description: 100 TABLET in 1 BOTTLE (54569-0452-0)

NDC Information of Isosorbide Dinitrate

NDC Code 54569-0452-0
Proprietary Name Isosorbide Dinitrate
Package Description 100 TABLET in 1 BOTTLE (54569-0452-0)
Product NDC 54569-0452
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880407
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name ISOSORBIDE DINITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Isosorbide Dinitrate


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