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Isosorbide Dinitrate
Isosorbide Dinitrate - 54868-2711-1 - (Isosorbide Dinitrate)
Drug Information of Isosorbide Dinitrate
| Product NDC: | 54868-2711 |
| Proprietary Name: | Isosorbide Dinitrate |
| Non Proprietary Name: | Isosorbide Dinitrate |
| Active Ingredient(s): | 40 mg/1 & nbsp; Isosorbide Dinitrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Isosorbide Dinitrate
| Product NDC: | 54868-2711 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040009 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950118 |
Package Information of Isosorbide Dinitrate
| Package NDC: | 54868-2711-1 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-2711-1) |
NDC Information of Isosorbide Dinitrate
| NDC Code | 54868-2711-1 |
| Proprietary Name | Isosorbide Dinitrate |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-2711-1) |
| Product NDC | 54868-2711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isosorbide Dinitrate |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19950118 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ISOSORBIDE DINITRATE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
