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Isosorbide Dinitrate - 0781-1635-13 - (Isosorbide Dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 0781-1635
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: 0781-1635
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086221
Marketing Category: ANDA
Start Marketing Date: 19880107

Package Information of Isosorbide Dinitrate

Package NDC: 0781-1635-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-1635-13) > 10 TABLET in 1 BLISTER PACK

NDC Information of Isosorbide Dinitrate

NDC Code 0781-1635-13
Proprietary Name Isosorbide Dinitrate
Package Description 10 BLISTER PACK in 1 CARTON (0781-1635-13) > 10 TABLET in 1 BLISTER PACK
Product NDC 0781-1635
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880107
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name ISOSORBIDE DINITRATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isosorbide Dinitrate


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