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- INJECTABLE;INJECTION - 25MG/10ML (2.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
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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