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Nitroglycerin
Nitroglycerin - 62175-123-01 - (Nitroglycerin)
Drug Information of Nitroglycerin
| Product NDC: | 62175-123 |
| Proprietary Name: | Nitroglycerin |
| Non Proprietary Name: | Nitroglycerin |
| Active Ingredient(s): | 20.8 mg/1 & nbsp; Nitroglycerin |
| Administration Route(s): | TRANSDERMAL |
| Dosage Form(s): | FILM, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nitroglycerin
| Product NDC: | 62175-123 |
| Labeler Name: | Kremers Urban Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075115 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040810 |
Package Information of Nitroglycerin
| Package NDC: | 62175-123-01 |
| Package Description: | 30 FILM, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (62175-123-01) |
NDC Information of Nitroglycerin
| NDC Code | 62175-123-01 |
| Proprietary Name | Nitroglycerin |
| Package Description | 30 FILM, EXTENDED RELEASE in 1 BOX, UNIT-DOSE (62175-123-01) |
| Product NDC | 62175-123 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nitroglycerin |
| Dosage Form Name | FILM, EXTENDED RELEASE |
| Route Name | TRANSDERMAL |
| Start Marketing Date | 20040810 |
| Marketing Category Name | ANDA |
| Labeler Name | Kremers Urban Pharmaceuticals Inc. |
| Substance Name | NITROGLYCERIN |
| Strength Number | 20.8 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |
