| NDC Code | 66267-676-30 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (66267-676-30) |
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| Product NDC | 66267-676 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20070406 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA086242 |
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| Manufacturer | NuCare Pharmaceuticals, Inc. |
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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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