Product NDC: | 0143-1765 |
Proprietary Name: | Isosorbide Dinitrate |
Non Proprietary Name: | Isosorbide Dinitrate |
Active Ingredient(s): | 2.5 mg/1 & nbsp; Isosorbide Dinitrate |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0143-1765 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA086054 |
Marketing Category: | ANDA |
Start Marketing Date: | 19781201 |
Package NDC: | 0143-1765-01 |
Package Description: | 100 TABLET in 1 BOTTLE (0143-1765-01) |
NDC Code | 0143-1765-01 |
Proprietary Name | Isosorbide Dinitrate |
Package Description | 100 TABLET in 1 BOTTLE (0143-1765-01) |
Product NDC | 0143-1765 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Isosorbide Dinitrate |
Dosage Form Name | TABLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 19781201 |
Marketing Category Name | ANDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | ISOSORBIDE DINITRATE |
Strength Number | 2.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |