| NDC Code | 0641-6231-25 |
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| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (0641-6231-25) / 20 mL in 1 VIAL, SINGLE-DOSE (0641-6231-01) |
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| Product NDC | 0641-6231 |
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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 | 20201218 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213667 |
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| Manufacturer | Hikma Pharmaceuticals USA Inc. |
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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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