
USFDA APPLICATION NUMBER - 19734 / DOSAGE - INJECTABLE;INJECTION - 25MG/10ML (2.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| NICARDIPINE HYDROCHLORIDE(UNII: K5BC5011K3) (NICARDIPINE - UNII:CZ5312222S) | NICARDIPINE HYDROCHLORIDE | 0.1mg in 1 | 0.1mg in 1 |