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Isosorbide Sublingual
Isosorbide Sublingual - 60429-109-01 - (Isosorbide Dinitrate)
Drug Information of Isosorbide Sublingual
| Product NDC: | 60429-109 |
| Proprietary Name: | Isosorbide Sublingual |
| Non Proprietary Name: | Isosorbide Dinitrate |
| Active Ingredient(s): | 5 mg/1 & nbsp; Isosorbide Dinitrate |
| Administration Route(s): | SUBLINGUAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Isosorbide Sublingual
| Product NDC: | 60429-109 |
| Labeler Name: | Golden State Medical Supply, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA086055 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19871102 |
Package Information of Isosorbide Sublingual
| Package NDC: | 60429-109-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (60429-109-01) |
NDC Information of Isosorbide Sublingual
| NDC Code | 60429-109-01 |
| Proprietary Name | Isosorbide Sublingual |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (60429-109-01) |
| Product NDC | 60429-109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Isosorbide Dinitrate |
| Dosage Form Name | TABLET |
| Route Name | SUBLINGUAL |
| Start Marketing Date | 19871102 |
| Marketing Category Name | ANDA |
| Labeler Name | Golden State Medical Supply, Inc. |
| Substance Name | ISOSORBIDE DINITRATE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
