| Product NDC: | 49349-883 |
| Proprietary Name: | Nitrostat |
| Non Proprietary Name: | Nitroglycerin |
| Active Ingredient(s): | .4 mg/1 & nbsp; Nitroglycerin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49349-883 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021134 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120302 |
| Package NDC: | 49349-883-40 |
| Package Description: | 25 TABLET in 1 VIAL (49349-883-40) |
| NDC Code | 49349-883-40 |
| Proprietary Name | Nitrostat |
| Package Description | 25 TABLET in 1 VIAL (49349-883-40) |
| Product NDC | 49349-883 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nitroglycerin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120302 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | NITROGLYCERIN |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |