| NDC Code | 48433-309-10 |
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| Package Description | 100 POUCH in 1 BOX, UNIT-DOSE (48433-309-10) > 1 TABLET, FILM COATED in 1 POUCH (48433-309-01) |
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| Product NDC | 48433-309 |
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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 | 20140930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA086242 |
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| Manufacturer | Safecor Health, LLC |
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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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