Isordil - 64455-192-01 - (isosorbide dinitrate)

Alphabetical Index


Drug Information of Isordil

Product NDC: 64455-192
Proprietary Name: Isordil
Non Proprietary Name: isosorbide dinitrate
Active Ingredient(s): 40    mg/1 & nbsp;   isosorbide dinitrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Isordil

Product NDC: 64455-192
Labeler Name: BTA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA012093
Marketing Category: NDA
Start Marketing Date: 20091001

Package Information of Isordil

Package NDC: 64455-192-01
Package Description: 100 TABLET in 1 BOTTLE (64455-192-01)

NDC Information of Isordil

NDC Code 64455-192-01
Proprietary Name Isordil
Package Description 100 TABLET in 1 BOTTLE (64455-192-01)
Product NDC 64455-192
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name isosorbide dinitrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091001
Marketing Category Name NDA
Labeler Name BTA Pharmaceuticals, Inc.
Substance Name ISOSORBIDE DINITRATE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Isordil


General Information