Isosorbide - 52125-059-02 - (ISOSORBIDE MONONITRATE)

Alphabetical Index


Drug Information of Isosorbide

Product NDC: 52125-059
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Isosorbide

Product NDC: 52125-059
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076813
Marketing Category: ANDA
Start Marketing Date: 20120917

Package Information of Isosorbide

Package NDC: 52125-059-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-059-02)

NDC Information of Isosorbide

NDC Code 52125-059-02
Proprietary Name Isosorbide
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-059-02)
Product NDC 52125-059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ISOSORBIDE MONONITRATE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120917
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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


General Information