Isosorbide - 59115-129-25 - (Isosorbide Dinitrate)

Alphabetical Index


Drug Information of Isosorbide

Product NDC: 59115-129
Proprietary Name: Isosorbide
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

Product NDC: 59115-129
Labeler Name: Hikma Pharmaceutical
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086066
Marketing Category: ANDA
Start Marketing Date: 19781201

Package Information of Isosorbide

Package NDC: 59115-129-25
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (59115-129-25)

NDC Information of Isosorbide

NDC Code 59115-129-25
Proprietary Name Isosorbide
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (59115-129-25)
Product NDC 59115-129
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 Hikma Pharmaceutical
Substance Name ISOSORBIDE DINITRATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isosorbide


General Information