NDC Code | 35356-972-60 |
Package Description | 60 TABLET in 1 BOTTLE (35356-972-60) |
Product NDC | 35356-972 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydralazine Hydrochloride |
Non-Proprietary Name | Hydralazine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20090601 |
Marketing Category Name | ANDA |
Application Number | ANDA090527 |
Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | HYDRALAZINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |