Home > National Drug Code (NDC) > isosorbide mononitrate

isosorbide mononitrate - 63629-1424-1 - (isosorbide mononitrate)

Alphabetical Index


Drug Information of isosorbide mononitrate

Product NDC: 63629-1424
Proprietary Name: isosorbide mononitrate
Non Proprietary Name: isosorbide mononitrate
Active Ingredient(s): 30    mg/1 & nbsp;   isosorbide mononitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of isosorbide mononitrate

Product NDC: 63629-1424
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075155
Marketing Category: ANDA
Start Marketing Date: 19981030

Package Information of isosorbide mononitrate

Package NDC: 63629-1424-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1424-1)

NDC Information of isosorbide mononitrate

NDC Code 63629-1424-1
Proprietary Name isosorbide mononitrate
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1424-1)
Product NDC 63629-1424
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isosorbide mononitrate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19981030
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ISOSORBIDE MONONITRATE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of isosorbide mononitrate


General Information