| NDC Code | 0615-0532-39 |
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| Package Description | 30 TABLET in 1 BLISTER PACK (0615-0532-39) |
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| Product NDC | 0615-0532 |
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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 | 19800227 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA086962 |
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| Manufacturer | NCS HealthCare of KY, Inc dba Vangard Labs |
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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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