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Isosorbide Dinitrate - 0781-1695-13 - (Isosorbide Dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 0781-1695
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: 0781-1695
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089367
Marketing Category: ANDA
Start Marketing Date: 19880407

Package Information of Isosorbide Dinitrate

Package NDC: 0781-1695-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-1695-13) > 10 TABLET in 1 BLISTER PACK

NDC Information of Isosorbide Dinitrate

NDC Code 0781-1695-13
Proprietary Name Isosorbide Dinitrate
Package Description 10 BLISTER PACK in 1 CARTON (0781-1695-13) > 10 TABLET in 1 BLISTER PACK
Product NDC 0781-1695
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880407
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name ISOSORBIDE DINITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isosorbide Dinitrate


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