Monoket - 0091-3620-18 - (isosorbide mononitrate)

Alphabetical Index


Drug Information of Monoket

Product NDC: 0091-3620
Proprietary Name: Monoket
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 Monoket

Product NDC: 0091-3620
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020215
Marketing Category: NDA
Start Marketing Date: 19930630

Package Information of Monoket

Package NDC: 0091-3620-18
Package Description: 180 TABLET in 1 BOTTLE (0091-3620-18)

NDC Information of Monoket

NDC Code 0091-3620-18
Proprietary Name Monoket
Package Description 180 TABLET in 1 BOTTLE (0091-3620-18)
Product NDC 0091-3620
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
Labeler Name UCB, Inc.
Substance Name ISOSORBIDE MONONITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Monoket


General Information