| NDC Code | 51662-1648-3 |
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| Package Description | 25 POUCH in 1 CASE (51662-1648-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1648-2) / 1 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 51662-1648 |
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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, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRAVENOUS |
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| Start Marketing Date | 19970630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040136 |
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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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