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Nitrolingual
Nitrolingual - 21695-768-49 - (nitroglycerin)
Drug Information of Nitrolingual
| Product NDC: | 21695-768 |
| Proprietary Name: | Nitrolingual |
| Non Proprietary Name: | nitroglycerin |
| Active Ingredient(s): | 400 ug/1 & nbsp; nitroglycerin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nitrolingual
| Product NDC: | 21695-768 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018705 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19851031 |
Package Information of Nitrolingual
| Package NDC: | 21695-768-49 |
| Package Description: | 60 SPRAY in 1 BOTTLE (21695-768-49) |
NDC Information of Nitrolingual
| NDC Code | 21695-768-49 |
| Proprietary Name | Nitrolingual |
| Package Description | 60 SPRAY in 1 BOTTLE (21695-768-49) |
| Product NDC | 21695-768 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nitroglycerin |
| Dosage Form Name | SPRAY |
| Route Name | ORAL |
| Start Marketing Date | 19851031 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | NITROGLYCERIN |
| Strength Number | 400 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |
