NDC Code | 76237-172-30 |
Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-172-30) > 5 TABLET in 1 BLISTER PACK |
Product NDC | 76237-172 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Hydralazine Hydrochloride |
Non-Proprietary Name | Hydralazine Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20111202 |
Marketing Category Name | ANDA |
Application Number | ANDA087836 |
Manufacturer | McKesson Contract Packaging |
Substance Name | HYDRALAZINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |