| NDC Code | 51662-1388-1 |
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| Package Description | 1 mL in 1 VIAL, SINGLE-DOSE (51662-1388-1) |
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| Product NDC | 51662-1388 |
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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 | INJECTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 20191007 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040730 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | HYDRALAZINE HYDROCHLORIDE |
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| Strength | 20 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
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