Product NDC: | 68462-147 |
Proprietary Name: | Nitroglycerin |
Non Proprietary Name: | Nitroglycerin |
Active Ingredient(s): | .6 mg/1 & nbsp; Nitroglycerin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68462-147 |
Labeler Name: | Glenmark Generics Inc., USA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED OTHER |
Start Marketing Date: | 20050303 |
Package NDC: | 68462-147-01 |
Package Description: | 100 TABLET in 1 BOTTLE (68462-147-01) |
NDC Code | 68462-147-01 |
Proprietary Name | Nitroglycerin |
Package Description | 100 TABLET in 1 BOTTLE (68462-147-01) |
Product NDC | 68462-147 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nitroglycerin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20050303 |
Marketing Category Name | UNAPPROVED OTHER |
Labeler Name | Glenmark Generics Inc., USA |
Substance Name | NITROGLYCERIN |
Strength Number | .6 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |