| NDC Code | 68788-6917-2 |
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| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (68788-6917-2) |
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| Product NDC | 68788-6917 |
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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 | 20170228 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA086242 |
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| Manufacturer | Preferred Pharmaceuticals Inc |
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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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