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Dilatrate
Dilatrate - 52244-920-10 - (Isosorbide Dinitrate)
Drug Information of Dilatrate
| Product NDC: | 52244-920 |
| Proprietary Name: | Dilatrate |
| Non Proprietary Name: | Isosorbide Dinitrate |
| Active Ingredient(s): | 40 mg/1 & nbsp; Isosorbide Dinitrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dilatrate
| Product NDC: | 52244-920 |
| Labeler Name: | Actient Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019790 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120215 |
Package Information of Dilatrate
| Package NDC: | 52244-920-10 |
| Package Description: | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (52244-920-10) |
NDC Information of Dilatrate
| NDC Code | 52244-920-10 |
| Proprietary Name | Dilatrate |
| Package Description | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (52244-920-10) |
| Product NDC | 52244-920 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isosorbide Dinitrate |
| Dosage Form Name | CAPSULE, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120215 |
| Marketing Category Name | NDA |
| Labeler Name | Actient Pharmaceuticals, LLC |
| Substance Name | ISOSORBIDE DINITRATE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE] |
