| NDC Code | 68462-341-05 |
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| Package Description | 500 TABLET in 1 BOTTLE (68462-341-05) |
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| Product NDC | 68462-341 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydralazine Hydrochloride |
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| Non-Proprietary Name | Hydralazine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20090529 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090527 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | HYDRALAZINE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
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