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Isosorbide Dinitrate - 49349-663-02 - (Isosorbide Dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 49349-663
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: 49349-663
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086221
Marketing Category: ANDA
Start Marketing Date: 20110310

Package Information of Isosorbide Dinitrate

Package NDC: 49349-663-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-663-02)

NDC Information of Isosorbide Dinitrate

NDC Code 49349-663-02
Proprietary Name Isosorbide Dinitrate
Package Description 30 TABLET in 1 BLISTER PACK (49349-663-02)
Product NDC 49349-663
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110310
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ISOSORBIDE DINITRATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isosorbide Dinitrate


General Information