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isosorbide mononitrate - 62175-107-01 - (isosorbide mononitrate)

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Drug Information of isosorbide mononitrate

Product NDC: 62175-107
Proprietary Name: isosorbide mononitrate
Non Proprietary Name: isosorbide mononitrate
Active Ingredient(s): 20    mg/1 & nbsp;   isosorbide mononitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of isosorbide mononitrate

Product NDC: 62175-107
Labeler Name: Kremers Urban Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020215
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19930630

Package Information of isosorbide mononitrate

Package NDC: 62175-107-01
Package Description: 100 TABLET in 1 BOTTLE (62175-107-01)

NDC Information of isosorbide mononitrate

NDC Code 62175-107-01
Proprietary Name isosorbide mononitrate
Package Description 100 TABLET in 1 BOTTLE (62175-107-01)
Product NDC 62175-107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isosorbide mononitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930630
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Kremers Urban Pharmaceuticals Inc.
Substance Name ISOSORBIDE MONONITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of isosorbide mononitrate


General Information