Product NDC: | 49884-020 |
Proprietary Name: | Isosorbide Dinitrate |
Non Proprietary Name: | isosorbide dinitrate |
Active Ingredient(s): | 5 mg/1 & nbsp; isosorbide dinitrate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49884-020 |
Labeler Name: | Par Pharmaceutical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA086923 |
Marketing Category: | ANDA |
Start Marketing Date: | 19791213 |
Package NDC: | 49884-020-10 |
Package Description: | 1000 TABLET in 1 BOTTLE (49884-020-10) |
NDC Code | 49884-020-10 |
Proprietary Name | Isosorbide Dinitrate |
Package Description | 1000 TABLET in 1 BOTTLE (49884-020-10) |
Product NDC | 49884-020 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | isosorbide dinitrate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19791213 |
Marketing Category Name | ANDA |
Labeler Name | Par Pharmaceutical Inc. |
Substance Name | ISOSORBIDE DINITRATE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |