| NDC Code | 54569-0517-1 | 
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			| Package Description | 60 TABLET in 1 BOTTLE (54569-0517-1) | 
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			| Product NDC | 54569-0517 | 
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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 | 20100101 | 
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			| Marketing Category Name | ANDA | 
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			| Application Number | ANDA040901 | 
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			| Manufacturer | A-S Medication Solutions LLC | 
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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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