| NDC Code | 0143-2230-10 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0143-2230-10) |
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| Product NDC | 0143-2230 |
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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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| End Marketing Date | 20201231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076813 |
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| Manufacturer | Hikma Pharmaceuticals USA Inc. |
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| Substance Name | ISOSORBIDE MONONITRATE |
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| Strength | 30 |
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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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