Isosorbide - 55154-7470-9 - (Isosorbide Dinitrate)

Alphabetical Index


Drug Information of Isosorbide

Product NDC: 55154-7470
Proprietary Name: Isosorbide
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

Product NDC: 55154-7470
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086066
Marketing Category: ANDA
Start Marketing Date: 19871029

Package Information of Isosorbide

Package NDC: 55154-7470-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-7470-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Isosorbide

NDC Code 55154-7470-9
Proprietary Name Isosorbide
Package Description 6 BLISTER PACK in 1 CARTON (55154-7470-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-7470
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19871029
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name ISOSORBIDE DINITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isosorbide


General Information