| NDC Code | 64380-735-07 |
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| Package Description | 500 TABLET in 1 BOTTLE (64380-735-07) |
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| Product NDC | 64380-735 |
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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 | 20130630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200770 |
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| Manufacturer | Strides Pharma Science Limited |
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| Substance Name | HYDRALAZINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
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