| NDC Code | 63739-327-10 |
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| Package Description | 10 BLISTER PACK in 1 CASE (63739-327-10) / 10 TABLET in 1 BLISTER PACK |
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| Product NDC | 63739-327 |
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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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| End Marketing Date | 20260131 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200770 |
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| Manufacturer | McKesson Corporation dba SKY Packaging |
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| Substance Name | HYDRALAZINE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
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