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Isosorbide Mononitrate - 0143-1333-01 - (Isosorbide Mononitrate)

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Drug Information of Isosorbide Mononitrate

Product NDC: 0143-1333
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Isosorbide Mononitrate

Product NDC: 0143-1333
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075361
Marketing Category: ANDA
Start Marketing Date: 20001005

Package Information of Isosorbide Mononitrate

Package NDC: 0143-1333-01
Package Description: 100 TABLET, COATED in 1 BOTTLE (0143-1333-01)

NDC Information of Isosorbide Mononitrate

NDC Code 0143-1333-01
Proprietary Name Isosorbide Mononitrate
Package Description 100 TABLET, COATED in 1 BOTTLE (0143-1333-01)
Product NDC 0143-1333
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Mononitrate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20001005
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name ISOSORBIDE MONONITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isosorbide Mononitrate


General Information