Product NDC: | 0338-1049 |
Proprietary Name: | Nitroglycerin In Dextrose |
Non Proprietary Name: | Nitroglycerin |
Active Ingredient(s): | 20 mg/100mL & nbsp; Nitroglycerin |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0338-1049 |
Labeler Name: | Baxter Healthcare Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019970 |
Marketing Category: | NDA |
Start Marketing Date: | 19891229 |
Package NDC: | 0338-1049-02 |
Package Description: | 250 mL in 1 BOTTLE, GLASS (0338-1049-02) |
NDC Code | 0338-1049-02 |
Proprietary Name | Nitroglycerin In Dextrose |
Package Description | 250 mL in 1 BOTTLE, GLASS (0338-1049-02) |
Product NDC | 0338-1049 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nitroglycerin |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19891229 |
Marketing Category Name | NDA |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | NITROGLYCERIN |
Strength Number | 20 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |