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Isosorbide Dinitrate - 49884-022-01 - (isosorbide dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 49884-022
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: 49884-022
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087537
Marketing Category: ANDA
Start Marketing Date: 19811215

Package Information of Isosorbide Dinitrate

Package NDC: 49884-022-01
Package Description: 100 TABLET in 1 BOTTLE (49884-022-01)

NDC Information of Isosorbide Dinitrate

NDC Code 49884-022-01
Proprietary Name Isosorbide Dinitrate
Package Description 100 TABLET in 1 BOTTLE (49884-022-01)
Product NDC 49884-022
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isosorbide dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19811215
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
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


General Information