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ISOSORBIDE MONONITRATE - 13668-106-10 - (ISOSORBIDE MONONITRATE)

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Drug Information of ISOSORBIDE MONONITRATE

Product NDC: 13668-106
Proprietary Name: ISOSORBIDE MONONITRATE
Non Proprietary Name: ISOSORBIDE MONONITRATE
Active Ingredient(s): 120    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: 13668-106
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200495
Marketing Category: ANDA
Start Marketing Date: 20110603

Package Information of ISOSORBIDE MONONITRATE

Package NDC: 13668-106-10
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-106-10)

NDC Information of ISOSORBIDE MONONITRATE

NDC Code 13668-106-10
Proprietary Name ISOSORBIDE MONONITRATE
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-106-10)
Product NDC 13668-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ISOSORBIDE MONONITRATE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110603
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
Substance Name ISOSORBIDE MONONITRATE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ISOSORBIDE MONONITRATE


General Information