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Isosorbide Dinitrate - 49884-020-10 - (isosorbide dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 49884-020
Proprietary Name: Isosorbide Dinitrate
Non Proprietary Name: isosorbide dinitrate
Active Ingredient(s): 5    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: 49884-020
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086923
Marketing Category: ANDA
Start Marketing Date: 19791213

Package Information of Isosorbide Dinitrate

Package NDC: 49884-020-10
Package Description: 1000 TABLET in 1 BOTTLE (49884-020-10)

NDC Information of Isosorbide Dinitrate

NDC Code 49884-020-10
Proprietary Name Isosorbide Dinitrate
Package Description 1000 TABLET in 1 BOTTLE (49884-020-10)
Product NDC 49884-020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isosorbide dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19791213
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name ISOSORBIDE DINITRATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Isosorbide Dinitrate


General Information