| Product NDC: | 68788-9676 |
| Proprietary Name: | Nitrostat |
| Non Proprietary Name: | nitroglycerin |
| Active Ingredient(s): | .4 mg/1 & nbsp; nitroglycerin |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68788-9676 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021134 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130515 |
| Package NDC: | 68788-9676-1 |
| Package Description: | 100 TABLET in 1 PACKAGE (68788-9676-1) |
| NDC Code | 68788-9676-1 |
| Proprietary Name | Nitrostat |
| Package Description | 100 TABLET in 1 PACKAGE (68788-9676-1) |
| Product NDC | 68788-9676 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nitroglycerin |
| Dosage Form Name | TABLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20130515 |
| Marketing Category Name | NDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | NITROGLYCERIN |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |