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Isosorbide Dinitrate - 0615-1560-39 - (Isosorbide Dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 0615-1560
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: 0615-1560
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086066
Marketing Category: ANDA
Start Marketing Date: 19781201

Package Information of Isosorbide Dinitrate

Package NDC: 0615-1560-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-1560-39)

NDC Information of Isosorbide Dinitrate

NDC Code 0615-1560-39
Proprietary Name Isosorbide Dinitrate
Package Description 30 TABLET in 1 BLISTER PACK (0615-1560-39)
Product NDC 0615-1560
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 NCS HealthCare of KY, Inc dba Vangard Labs
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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