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Isosorbide Dinitrate - 63629-2573-1 - (Isosorbide Dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 63629-2573
Proprietary Name: Isosorbide Dinitrate
Non Proprietary Name: Isosorbide Dinitrate
Active Ingredient(s): 10    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: 63629-2573
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086066
Marketing Category: ANDA
Start Marketing Date: 19781201

Package Information of Isosorbide Dinitrate

Package NDC: 63629-2573-1
Package Description: 30 TABLET in 1 BOTTLE (63629-2573-1)

NDC Information of Isosorbide Dinitrate

NDC Code 63629-2573-1
Proprietary Name Isosorbide Dinitrate
Package Description 30 TABLET in 1 BOTTLE (63629-2573-1)
Product NDC 63629-2573
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19781201
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ISOSORBIDE DINITRATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Isosorbide Dinitrate


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