| NDC Code | 68071-4689-3 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4689-3) |
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| Product NDC | 68071-4689 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Isosorbide |
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| Non-Proprietary Name | Isosorbide Mononitrate |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20060330 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076813 |
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| Manufacturer | NuCare Pharmaceuticals,Inc. |
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| Substance Name | ISOSORBIDE MONONITRATE |
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| Strength | 60 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Nitrate Vasodilator [EPC], Nitrates [CS], Vasodilation [PE] |
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