NDC Code | 51662-1482-1 |
Package Description | 10 mL in 1 VIAL (51662-1482-1) |
Product NDC | 51662-1482 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Nicardipine Hydrochloride |
Non-Proprietary Name | Nicardipine Hydrochloride |
Dosage Form | INJECTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20200201 |
Marketing Category Name | NDA |
Application Number | NDA022276 |
Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
Substance Name | NICARDIPINE HYDROCHLORIDE |
Strength | 25 |
Strength Unit | mg/10mL |
Pharmacy Classes | Calcium Channel Antagonists [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |