NDC Code | 35356-943-30 |
Package Description | 30 TABLET in 1 BOTTLE (35356-943-30) |
Product NDC | 35356-943 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydralazine Hydrochloride |
Non-Proprietary Name | Hydralazine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20100101 |
Marketing Category Name | ANDA |
Application Number | ANDA040901 |
Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | HYDRALAZINE HYDROCHLORIDE |
Strength | 50 |
Strength Unit | mg/1 |
Pharmacy Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |