Isosorbide - 55154-7465-9 - (Isosorbide mononitrate)

Alphabetical Index


Drug Information of Isosorbide

Product NDC: 55154-7465
Proprietary Name: Isosorbide
Non Proprietary Name: Isosorbide mononitrate
Active Ingredient(s): 30    mg/1 & nbsp;   Isosorbide mononitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Isosorbide

Product NDC: 55154-7465
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076813
Marketing Category: ANDA
Start Marketing Date: 20060330

Package Information of Isosorbide

Package NDC: 55154-7465-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-7465-9) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Isosorbide

NDC Code 55154-7465-9
Proprietary Name Isosorbide
Package Description 6 BLISTER PACK in 1 CARTON (55154-7465-9) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-7465
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide mononitrate
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060330
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name ISOSORBIDE MONONITRATE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isosorbide


General Information