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NDC 70710-1149-00 Isosorbide dinitrate 10 mg/1 Details
Isosorbide dinitrate 10 mg/1
Isosorbide dinitrate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals (USA) Inc.. The primary component is ISOSORBIDE DINITRATE.
MedlinePlus Drug Summary
Isosorbide immediate-release tablets are used for the management of angina (chest pain) in people who have coronary artery disease (narrowing of the blood vessels that supply blood to the heart). Isosorbide extended-release (long-acting) tablets and extended-release capsules are used for the management of chest pain in people who have coronary artery disease. Isosorbide can only be used to prevent angina; it cannot be used to treat an episode of angina once it has begun. Isosorbide is in a class of medications called vasodilators. It works by relaxing the blood vessels so the heart does not need to work as hard and therefore does not need as much oxygen.
Related Packages: 70710-1149-00Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Isosorbide
Product Information
| NDC | 70710-1149 |
|---|---|
| Product ID | 70710-1149_f2c34ec3-1ada-4f01-9cfe-07cfd7d781e0 |
| Associated GPIs | 32100020000310 |
| GCN Sequence Number | 000507 |
| GCN Sequence Number Description | isosorbide dinitrate TABLET 10 MG ORAL |
| HIC3 | A7B |
| HIC3 Description | VASODILATORS,CORONARY |
| GCN | 01942 |
| HICL Sequence Number | 000166 |
| HICL Sequence Number Description | ISOSORBIDE DINITRATE |
| Brand/Generic | Generic |
| Proprietary Name | Isosorbide dinitrate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Isosorbide dinitrate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | ISOSORBIDE DINITRATE |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Pharmaceutical Class | Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA213057 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70710-1149-00 (70710114900)
| NDC Package Code | 70710-1149-0 |
|---|---|
| Billing NDC | 70710114900 |
| Package | 1000 TABLET in 1 BOTTLE (70710-1149-0) |
| Marketing Start Date | 2019-11-25 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |