IMDUR - 0085-2028-01 - (isosorbide mononitrate)

Alphabetical Index


Drug Information of IMDUR

Product NDC: 0085-2028
Proprietary Name: IMDUR
Non Proprietary Name: isosorbide mononitrate
Active Ingredient(s): 60    mg/1 & nbsp;   isosorbide mononitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of IMDUR

Product NDC: 0085-2028
Labeler Name: Schering Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075155
Marketing Category: ANDA
Start Marketing Date: 20060105

Package Information of IMDUR

Package NDC: 0085-2028-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0085-2028-01)

NDC Information of IMDUR

NDC Code 0085-2028-01
Proprietary Name IMDUR
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0085-2028-01)
Product NDC 0085-2028
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isosorbide mononitrate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20060105
Marketing Category Name ANDA
Labeler Name Schering Corporation
Substance Name ISOSORBIDE MONONITRATE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of IMDUR


General Information