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Isosorbide Dinitrate - 0179-0086-70 - (Isosorbide Dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 0179-0086
Proprietary Name: Isosorbide Dinitrate
Non Proprietary Name: Isosorbide Dinitrate
Active Ingredient(s): 40    mg/1 & nbsp;   Isosorbide Dinitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Isosorbide Dinitrate

Product NDC: 0179-0086
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040723
Marketing Category: ANDA
Start Marketing Date: 20110315

Package Information of Isosorbide Dinitrate

Package NDC: 0179-0086-70
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0179-0086-70)

NDC Information of Isosorbide Dinitrate

NDC Code 0179-0086-70
Proprietary Name Isosorbide Dinitrate
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (0179-0086-70)
Product NDC 0179-0086
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Dinitrate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110315
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name ISOSORBIDE DINITRATE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isosorbide Dinitrate


General Information