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NITROGLYCERIN
NITROGLYCERIN - 59762-3304-3 - (nitroglycerin)
Drug Information of NITROGLYCERIN
| Product NDC: | 59762-3304 |
| Proprietary Name: | NITROGLYCERIN |
| Non Proprietary Name: | nitroglycerin |
| Active Ingredient(s): | .4 mg/1 & nbsp; nitroglycerin |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NITROGLYCERIN
| Product NDC: | 59762-3304 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021134 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20030408 |
Package Information of NITROGLYCERIN
| Package NDC: | 59762-3304-3 |
| Package Description: | 4 BOTTLE in 1 PACKAGE (59762-3304-3) > 25 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE |
NDC Information of NITROGLYCERIN
| NDC Code | 59762-3304-3 |
| Proprietary Name | NITROGLYCERIN |
| Package Description | 4 BOTTLE in 1 PACKAGE (59762-3304-3) > 25 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE |
| Product NDC | 59762-3304 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nitroglycerin |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 20030408 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | NITROGLYCERIN |
| Strength Number | .4 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |
