NICARDIPINE HYDROCHLORIDE
| Brand name | NICARDIPINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE |
|---|---|
| Active ingredient | NICARDIPINE HYDROCHLORIDE |
| Strength | 20MG/200ML (0.1MG/ML) |
| Dosage form | INJECTABLE |
| Route | INTRAVENOUS |
| Modality | Small molecule |
| FDA approval | September 2024 |
| Marketing status | RX |
Source: FDA Orange Book, layered on the CliffBio company graph. Cliff dates are the loss of exclusivity; estimates are projections, not legal advice.