Nicardipine Hydrochloride 70069-0875-10

Package NDC

70069-0875-10

Manufacturer: Somerset Therapeutics, Llc
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: April 20, 2026
Listing Expires: December 31, 2027
Application: ANDA220243

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Active Ingredients

Ingredient	Strength
Nicardipine Hydrochloride	.1 mg/mL

Drug Class

Calcium Channel Antagonists [MoA]Cytochrome P450 2C19 Inhibitors [MoA]Cytochrome P450 2C8 Inhibitors [MoA]

Selected Package

70069-0875-10Selected

10 POUCH in 1 CASE (70069-875-10) / 1 BAG in 1 POUCH (70069-875-01) / 200 mL in 1 BAG