| NDC Code | 68084-435-01 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (68084-435-01) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-435-11) |
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| Product NDC | 68084-435 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Isosorbide Mononitrate |
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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 | 20130708 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076813 |
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| Manufacturer | American Health Packaging |
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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 [Chemical/Ingredient],Vasodilation [PE] |
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