| NDC Code | 71209-016-11 |
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| Package Description | 1000 TABLET in 1 BOTTLE (71209-016-11) |
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| Product NDC | 71209-016 |
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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 | 20151229 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203845 |
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| Manufacturer | Cadila Pharmaceuticals Limited |
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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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