NDC Code | 68071-4490-3 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4490-3) |
Product NDC | 68071-4490 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydralazine Hydrochloride |
Non-Proprietary Name | Hydralazine Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20070406 |
Marketing Category Name | ANDA |
Application Number | ANDA086242 |
Manufacturer | NuCare Pharmaceuticals,Inc. |
Substance Name | HYDRALAZINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |