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USFDA APPLICATION NUMBER - 19734 / DOSAGE - INJECTABLE;INTRAVENOUS - 40MG/200ML (0.2MG/ML)
| 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 |
Inactive Ingredients
| Ingredient Name | Chiesi USA, Inc. | EKR Therapeutics | EKR Therapeutics, Inc. |
|---|---|---|---|
| CITRIC ACID MONOHYDRATE(2968PHW8QP) | |||
| DEXTROSE MONOHYDRATE(LX22YL083G) | |||
| SODIUM CHLORIDE(451W47IQ8X) | |||
| SODIUM HYDROXIDE(55X04QC32I) | |||
| SORBITOL(506T60A25R) |
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