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Isosorbide Dinitrate - 0143-1772-30 - (Isosorbide Dinitrate)

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Drug Information of Isosorbide Dinitrate

Product NDC: 0143-1772
Proprietary Name: Isosorbide Dinitrate
Non Proprietary Name: Isosorbide Dinitrate
Active Ingredient(s): 20    mg/1 & nbsp;   Isosorbide Dinitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Isosorbide Dinitrate

Product NDC: 0143-1772
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088088
Marketing Category: ANDA
Start Marketing Date: 19830426

Package Information of Isosorbide Dinitrate

Package NDC: 0143-1772-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (0143-1772-30)

NDC Information of Isosorbide Dinitrate

NDC Code 0143-1772-30
Proprietary Name Isosorbide Dinitrate
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (0143-1772-30)
Product NDC 0143-1772
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Isosorbide Dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19830426
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name ISOSORBIDE DINITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]

Complete Information of Isosorbide Dinitrate


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